Comparison Between Bupivacaine With and Without Fentanyl in Reducing Pain During Cesarean Delivery Under Spinal Anaesthesia

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-09-20

Study Completion Date

2023-04-13

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Spinal anaesthesia with hyperbaric bupivacaine is the most commonly used anesthetic technique for cesarean section. Delivery of baby during cesarean section requires traction of peritoneum and handling of intraperitoneal organs resulting in intraoperative visceral pain. The incidence of this intraoperative visceral pain can be reduced with higher dose of hyperbaric bupivacaine (12-15mg), but increasing the dose of bupivacaine increases the risk of high sensory block resulting to major hemodynamic adverse events like hypotension, bradycardia or may lead to fetal distress. Neuraxial administration of fentanyl added to bupivacaine has been proposed to intensify the sensory block without increasing sympathetic block and also improves the quality of intraoperative analgesia thus, reduces the incidence of intraoperative visceral pain. Several studies have convincingly demonstrated efficacy of intrathecal fentanyl of different doses in improving the intraoperative analgesic effect along with its associated clinical effects. However, there has been limited research conducted to compare the analgesic effects of intrathecal fentanyl of low dose in reducing visceral pain in cesarean delivery especially in our setting.

Therefore, in this study investigator aim to compare between hyperbaric bupivacaine alone with hyperbaric bupivacaine and fentanyl in reducing the visceral pain during cesarean sectionunder spinal anaesthesia.

In this study, term parturient undergoing cesarean delivery in spinal anesthesia will be allocated in 2 groups. One group will receive intrathecal hyperbaric bupivacaine whereas another interventional group will receive hyperbaric bupivacaine with addition of fentanyl. Visceral pain will be assessed in both group using numerical pain rating scale along with monitoring of vitals. Data will be collected and will be filled up in a master chart in Microsoft Excel. Statistical analysis will be done.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Comparison of the Time to the First Rescue Analgesic Among Parturients Receiving Intrathecal Additive Fentanyl or Intrathecal Fentanyl With TAP Block or TAP Block Alone for Elective Cesarean Sections Under Hyperbaric Bupivacaine Spinal Anesthesia

NCT05550597

Postoperative Pain Cesarean Section

COMPLETED NA

Comparison of Transversalis Fascia Plane Block and Erector Spinae Plane Blocks in Cesarean Section

NCT05117307

Pain Postoperative Pain

NOT_YET_RECRUITING NA

Use of Intrathecal Fentanyl and Development of Hyperalgesia in Patients Undergoing Elective Cesarean

NCT02387060

Complications; Cesarean Section

UNKNOWN PHASE4

Transversalis Fascia Plane Blocks for Analgesia Post-cesarean Delivery

NCT03236324

Cesarean Delivery

COMPLETED PHASE2

Hyperbaric Bupivacaine and Hyperbaric Levobupivacaine in C/S

NCT02025374

Health Care Drugs

COMPLETED PHASE4

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

All the pregnant women who are planned for cesarean section will be enrolled in the study and assessed for eligibility. Patients who does not meet the inclusion criteria or those who refuse to participate will be excluded from study . Other enrolled parturient who meet the eligible criteria will be randomized and allocated to two study groups by computer generated numbers that will be concealed in sequentially numbered, opaque sealed envelopes. A day prior to surgery, eligible patients will be explained in detail about the purpose of study, need, benefits and risks of procedure. They will be instructed on the method used for sensory and motor assessments. In addition they will be explained about numerical rating scale of pain, how to use it and rate it during intraoperative period. Written informed consent will be obtained during pre anaesthetic checkup. Patients will be counselled about fasting protocol and asked to remain nil per oral of 2 hours for clear liquid, 6 hours for light foods and 8 hours for fatty food. Before surgery, premedication will be done with Tablet Pantoprazole 40 mg and Tablet Metoclopramide 10 mg at 10 pm the day before surgery and 6 am in morning of surgery. In pre-delivery room, a peripheral intravenous (IV) line will be established with 18-G IV cannula. Preloading will be done with 10 ml/kg of Lactated Ringer's solution. Baseline blood pressure, mean arterial pressure, heart rate, respiratory rate, SpO2, fetal heart rate will be recorded in pre-delivery room. In the operation theater: Standard monitor including electrocardiography, noninvasive blood pressure monitoring and pulse oximetry will be attached. Patient will be positioned in sitting position. Painting of the patient's back with 10% povidine iodine and draping with sterile drapes will be done. Identification of intervertebral space will be done and the skin will be infiltrated with lidocaine 2% under all aseptic precautions.25-gauge Quincke's spinal needle will be introduced at L3-L4 intervertebral space using a midline approach in sitting position. After ensuring free flow of cerebrospinal fluid, study drug will be given over 10 - 15 sec. Study drugs would be prepared as: In group B, Inj. 0.5% hyperbaric bupivacaine 11mg (2.2ml) will be prepared. In group BF, Inj. 0.5% hyperbaric bupivacaine 10 mg (2ml) with addition of 10mcg (0.2ml) fentanyl with total volume of 2.2 ml will be prepared. Immediately after administration of spinal anesthesia, patient will be positioned supine with wedge under right hip and the time will be recorded as "time-zero".

Fetal heart rates will be noted. Patients will receive oxygen 3L/min via nasal cannula if SpO2 decreases to \<95%.NIBP and HR will be assessed every 3 minute following SAB for 15 minutes or until delivery of baby and thereafter every 5 minutes till the end of surgery. SpO2 and ECG were monitored continuously throughout the study period. Sensory level will be assessed bilaterally along the mid clavicular line using spirit soaked cotton until block reached upto T6 dermatome. Motor block will be assessed based on Modified Bromage Scale. Surgery will be allowed as soon as upper sensory level reaches T6 and Bromage scale of M3.Thereafter, the level will be checked every 2 min until maximal sensory block level is confirmed. Intra operative pain will be assessed whenever the patient complains of pain or discomfort during surgery. If somatic pain occur (at time of incision to skin or subcutaneous tissue), spinal anesthesia will be converted to general anesthesia and excluded from study. For visceral pain, patient will be asked to express the pain in Numerical Rating Scale (0-10).

Assessment of visceral pain will be mainly done during ;- Delivery of baby with fundal pressure application, exteriorization of uterus, handling of other intraperitoneal organs like bowels, adnexa so as to clear off the secretions and blood, suturing of visceral peritoneum, placement of uterus back to abdominal cavity after repair. Each time NRS is 4 or more it will be considered as inadequate analgesia and inj. Fentanyl 25 mcg will be given IV bolus. Investigator will wait for 3 min for its adequate effect. If still pain persists, then the dose of fentanyl will be increased to 1 mcg/kg. After 2 doses of fentanyl, if pain still persists then Inj. Ketamine 0.5mcg/kg IV will be given. If still pain is unbearable, general anesthesia will be administered. The need to convert to general anesthesia will be noted. Following delivery of the baby, Inj. oxytocin 3 IU will be administered bolus. Continuous infusion of oxytocin drip will be given as per need after communicating with obstetrician. APGAR score of the neonate will be evaluated at 1 minute and 5 minutes.

Hypotension will be promptly treated with intravenous fluid bolus (200 ml) and Inj.

Mephentermine 6mg IV boluses, which will be repeated if necessary. If bolus dose of Mephentermine exceeds 30mg then Inj. Phenylephrine 50 mcg IV will be given. Inj. Atropine 0.6mg will be given if bradycardia occurs. If respiratory depression occur, it will be recorded and managed as -if RR ≤10 breaths /minutes then physical stimulus will be given (tapping a patient's shoulder with calling her name ). If RR is still not increased or RR ≤ 8 breaths /minutes then Inj. Nalaoxone 0.4 mg IV will be given and will be repeated after 2-3 min if necessary. Dose of Naloxone will not be exceeded 10mg/ day. Postoperatively, follow up will be done every 15 minutes if any intraoperative adverse events is noted, otherwise every 1 hourly to assess for any hemodynamic changes and adverse events related to study drug upto 6 hours. Then, monitoring of vitals, urine output and pain management will be done upto 18 hours.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Visceral Pain

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants are assigned to study where two groups of treatments B and BF are given so that one group receives only B while another group receives only BF for the duration of study.

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Patients will be randomly distributed in the two groups using computed generated numbers that will be concealed in sequentially numbered, opaque sealed envelopes.

The envelopes will be opened by an attending nurse not involved in the study just before the procedure. The study drug will be prepared by the attending anesthesiologist/ resident who will perform the subarachnoid block. The assessment of pain and data collection, data analysis will be done by principle investigator who is blinded to procedure.

Thus, the patients and investigating and analyzing personal will be blinded to the procedure.

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group B (bupivacaine group)

Drug used: 0.5% hyperbaric bupivacaine heavy (8%dextrose) dose -11mg with volume of 2.2ml single administration, no repetition of intervention

Group Type ACTIVE_COMPARATOR

0.5% bupivacaine heavy

Intervention Type DRUG

Spinal anesthesia with 0.5% bupivacaine heavy at L3-L4 intervertebral space using Quincke's spinal needle in sitting position, single administration for each patient

Group BF(bupivacaine with fentanyl group)

Drug used:- 0.5% hyperbaric bupivacaine heavy (8%dextrose) dose -10mg, 2ml and fentanyl 10mg ,0.2ml with total volume of of 2.2ml single administration, no repetition of intervention

Group Type EXPERIMENTAL

0.5% bupivacaine heavy with fentanyl

Intervention Type DRUG

Spinal anesthesia with 0.5% bupivacaine heavy with fentanyl at L3-L4 intervertebral space using Quincke's spinal needle in sitting position, single administration for each patient

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

0.5% bupivacaine heavy

Spinal anesthesia with 0.5% bupivacaine heavy at L3-L4 intervertebral space using Quincke's spinal needle in sitting position, single administration for each patient

Intervention Type DRUG

0.5% bupivacaine heavy with fentanyl

Spinal anesthesia with 0.5% bupivacaine heavy with fentanyl at L3-L4 intervertebral space using Quincke's spinal needle in sitting position, single administration for each patient

Intervention Type DRUG

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Anawin Heavy 0.5% anawin heavy 0.5% + Trofentyl

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* ASA PS II
* Elective cesarean deliveries under SAB
* Age ≥18 years
* Term pregnancy ≥37 weeks of gestation
* Height ≥ 150 cm

Exclusion Criteria

* Patients with neurological, psychiatric, cardiopulmonary, hepatorenal diseases, coagulopathy
* Patient refusal to participate
* Allergy or hypersensitivity to bupivacaine or fentanyl
* Patients with communication problem

Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No