To Study and Evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for Post-operative Pain in Cesarean Section Patients Using Primary Relief v 2.0

NCT ID: NCT03829774

Last Updated: 2019-02-05

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 22 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-01-02
• Study Completion Date: 2019-07-31

Brief Summary

To study and evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for post-operative pain in Cesarean Section patients using First Relief

Conditions

Cesarean Section; Dehiscence

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Primary Relief v 2.0 Device

The test product or device called Primary Relief v 2.0 device will be used for the study. The study will be conducted for a period of two to three months with the treatment period of 3 - 4 days i.e single treatment (installation). The additional time taken will be to define the characteristics of the patient population and to recruit appropriate patients. Finally, there will be a data analysis and report writing period. Overall, the study is expected to 3 months. The device will be placed onto the auricle part of the ear for percutaneous electrical nerve stimulation.

Group Type: EXPERIMENTAL

Primary Relief v 2.0

Intervention Type: DEVICE

The test product or device called Primary Relief v 2.0 will be used for the study. The study will be conducted for a period of two to three months with the treatment period of 3 - 4 days i.e single treatment (installation). The additional time taken will be to define the characteristics of the patient population and to recruit appropriate patients. Finally, there will be a data analysis and report writing period. Overall, the study is expected to 3 months. The device will be placed onto the auricle part of the ear for percutaneous electrical nerve stimulation.

Paracetamol

A control group, receiving a standard treatment as follows: primary choice of analgesic was intravenous Paracetamol , 1 gram, and if the pain relief was inadequate, diclofenac inj. If pain persisted in spite of these measures, 50 mg tramadol was administered intravenously

Group Type: PLACEBO_COMPARATOR

Paracetamol

Intervention Type: DRUG

A control group, receiving a standard treatment as follows: primary choice of analgesic was intravenous paracetamol, 1 gram, and if the pain relief was inadequate, diclofenac inj. If pain persisted in spite of these measures, 50 mg tramadol was administered intravenously

Interventions

Primary Relief v 2.0

The test product or device called Primary Relief v 2.0 will be used for the study. The study will be conducted for a period of two to three months with the treatment period of 3 - 4 days i.e single treatment (installation). The additional time taken will be to define the characteristics of the patient population and to recruit appropriate patients. Finally, there will be a data analysis and report writing period. Overall, the study is expected to 3 months. The device will be placed onto the auricle part of the ear for percutaneous electrical nerve stimulation.

Intervention Type: DEVICE

Paracetamol

A control group, receiving a standard treatment as follows: primary choice of analgesic was intravenous paracetamol, 1 gram, and if the pain relief was inadequate, diclofenac inj. If pain persisted in spite of these measures, 50 mg tramadol was administered intravenously

Intervention Type: DRUG

Other Intervention Names

Percutaeneous Nerve Field Stimulator Neurostimulator; Standard Drug Treatment for Postoperative pain

Eligibility Criteria

Inclusion Criteria

1. Age range between 22 - 35 years

2. Patient willing to undergo C-section surgery

3. Patient having pains after one hour of post C-Section surgery

4. Patients who is conscious and oriented for device installation after anesthetic effect

5. Patient who completed required clinical and biochemical investigations as deemed necessary by the gynecologist after post C - section surgery.

6. No previous poor obstetrical outcome

7. No experience in Han's Acupoint nerve stimulator and TENS for other reasons.

8. Term pregnancy (> 37 weeks of gestation).

9. Understands and is willing to participate in the clinical study and can comply with study procedures.

10. Normal cognitive and communicative ability as judged by clinical assessment and ability to complete self-reported questionnaires.

Exclusion Criteria

1. Had been diagnosed with other diseases such as preoperative presence of maternal mental, neurological disease, affecting evaluation of pains and disease condition.

2. Had combined with gestational hypertension, gestational diabetes, gestational thyroid disease.

3. Had taken analgesic drugs

4. Had used diazepam, piperazine hydrochloride or other sedative, analgesic drugs in the stage of labor.

5. Were overweight or low pregnancy weight, Body mass index (< 18.5 or >25 kg/m2).

6. Patients who are not agreeing to receive painless labor and not sign the informed consent form.

7. Neonatal problem requiring immediate separation from the mother for medical care or NICU admittance.

8. Severe placental abruption.

9. Hydrops (accumulation of fluid or edema in fetus body tissue and cavities) if secondary to anemia or heart failure.

10. Known twin to twin transfusion syndrome (TTS).

11. Congenital anomalies that may hamper the procedure (gastroschisis, amphalacele, spina bifida).

12. Home birth.

13. Severe mental health problem

14. Hearing impairment.

15. Legal abortion

16. Twin pregnancy

17. Instrumental birth

18. Uterine anomalies with contraindication for vaginal birth. Eg: previous opening of uterine cavity, myomectomy, congenital abnormalities.

19. Placenta anomalies.

20. Placenta praevia, suspected acreta, increta, percreta especially after previous caesarean.

21. Fetal abnormalities, growth restriction.

22. Maternal complication with surgery.

23. Subjects on any investigational drug(s) or therapeutic device(s) within 30 days preceding screening; or subject or physician anticipates use of any of these therapies by the subject during the course of the study

24. Previous participation in the Treatment Phase of this Protocol

25. Malignant disease not in remission for five years or more that has been medically or surgically treated without evidence of metastases

26. Presence of one or more medical conditions, as determined by medical history, which seriously compromises the subject's ability to complete the study, including history of poor adherence with medical treatment, unstable pain intensity or pain medications 6 weeks prior to the study, renal, hepatic, hematologic, active auto-immune or immune diseases that, in the opinion of the Investigator, would make the subject an inappropriate candidate for this study: a) One or more abnormal blood biochemistry analyte result that is ≥ 3 times that of the upper limit of the normal range

27. Known history of having Acquired Immunodeficiency Syndrome (AIDS) or with a history known to be infected with Human Immunodeficiency Virus (HIV)

28. American Heart Association (AHA) Class III and IV congestive heart failure (CHF), as defined by the following criteria: a) Class III: Symptoms with moderate exertion b) Class IV: Symptoms at rest or c) Cardiac pacemakers.

29. Subjects with a diagnosis of psychiatric disorders such as major depressive disorder, bipolar disorder, obsessive compulsive disorder, generalized anxiety, dysthymia or suicidality/suicide ideation

30. Subjects not willing to undergo treatment before discharge from the hospital.

• Minimum Eligible Age: 22 Years
• Maximum Eligible Age: 35 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

DyAnsys, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Clinic

Warangal, Telangana, India

Site Status: RECRUITING

Countries

India

Central Contacts

Balachandran V, MD

Role: CONTACT

v.balachandran@dyansys.com

+91 9946452707

Hariharan A, B.Tech

Role: CONTACT

a.hariharan@dyansys.com

+91 8124147672

Facility Contacts

Balachandran V, MD

Role: primary

v.balachandaran@dyansys.com

9496452707

Robin M, GNM

Role: backup

8722627172

References

Zimpel SA, Torloni MR, Porfirio GJ, Flumignan RL, da Silva EM. Complementary and alternative therapies for post-caesarean pain. Cochrane Database Syst Rev. 2020 Sep 1;9(9):CD011216. doi: 10.1002/14651858.CD011216.pub2.

Reference Type: DERIVED

PMID: 32871021 (View on PubMed)

Other Identifiers

CS/PRv2.0/C-Sec/2019

Identifier Type: -

Identifier Source: org_study_id