Comparsion of IV Dexmedetomidine, Tramdol and Ketamine for Post Spinal Anesthesia Shivering.

NCT ID: NCT05311722

Last Updated: 2022-04-05

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

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE3

Total Enrollment

71 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-04-30

Study Completion Date

2023-02-20

Brief Summary

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To study control of post spinal shivering in patients undergoing lower segment cesarean section using dexmedetomidine, tramadol and ketamine

Detailed Description

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Its a Comparison of drugs for a better control of post spinal shivering in patietns underwent cesarean section.using grades of shivering (0-4)patients will be assessed

Conditions

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Post-Surgical Complication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

3 drugs were given to patients
Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Participants

Study Groups

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Dexmedetomidine

Inj.dexmedetomidine 0.5mcg/kg diluted in 10ml N/s given as iv infusion over 10 minutes

Group Type EXPERIMENTAL

Dexmedetomidine

Intervention Type DRUG

Inj dexmedetomidine, will be given in infusion over 10 mins and their effect on post spinal shivering will be assessed.

Ketamine

Inj.ketamine 0.5mg/kg diluted in 10ml N/s given as iv infusion over 10 minutes

Group Type EXPERIMENTAL

Ketamine

Intervention Type DRUG

Ketamine

Tramadol

Inj.tramadol 0.5mg/kg diluted in 10ml N/s given as iv infusion over 10 minutes

Group Type EXPERIMENTAL

Tramadol

Intervention Type DRUG

Tramadol

Interventions

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Dexmedetomidine

Inj dexmedetomidine, will be given in infusion over 10 mins and their effect on post spinal shivering will be assessed.

Intervention Type DRUG

Ketamine

Ketamine

Intervention Type DRUG

Tramadol

Tramadol

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Woman of age 18-60
* Pregnant woman in outdoor patient department and emergency

Exclusion Criteria

* patient. with history of hypersensitivity to opioids,
* ketamine or bupivacaine
* History of cardiovascular disease,
* Hypertension,
* psychosis,
* antepartum hemorrhage,
* cord prolapse,
* fetal distress
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Sheikh Zayed Medical College

OTHER_GOV

Sponsor Role lead

Responsible Party

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Obaid ur Rehman

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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Obaid ur rehman Reman, Mbbs

Role: CONTACT

03335817980

Other Identifiers

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ORehman

Identifier Type: -

Identifier Source: org_study_id

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