Control of post spinal shivering dexmedetomidine, tramadol and ketamine for control of post spinal shivering.
Comparsion of IV Dexmedetomidine, Tramdol and Ketamine for Post Spinal Anesthesia Shivering.
Brief Summary
To study control of post spinal shivering in patients undergoing lower segment cesarean section using dexmedetomidine, tramadol and ketamine
Intervention / Treatment
3 drugs were given to patients
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Dexmedetomidine (DRUG)Inj dexmedetomidine, will be given in infusion over 10 mins and their effect on post spinal shivering will be assessed.
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Ketamine (DRUG)
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Tramadol (DRUG)
Condition or Disease
- Post-Surgical Complication
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Not yet recruiting |
Study results: | No Results Available |
Age: | 18 Years to 60 Years |
Enrollment: | 71 (ESTIMATED) |
Allocation: | Randomized |
Primary Purpose: | Health Services Research |
MaskingSINGLE:
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Clinical Trial Dates
Start date: | Apr 30, 2022 | ESTIMATED |
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Primary Completion: | Dec 31, 2022 | ESTIMATED |
Completion Date: | Feb 20, 2023 | ESTIMATED |
Study First Posted: | Apr 05, 2022 | ACTUAL |
Last Updated: | Apr 04, 2022 |
Sponsors / Collaborators
Lead Sponsor:
N/A
Responsible Party:
N/A
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
Participant Groups
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Inj.dexmedetomidine 0.5mcg/kg diluted in 10ml N/s given as iv infusion over 10 minutes
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Inj.ketamine 0.5mg/kg diluted in 10ml N/s given as iv infusion over 10 minutes
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Inj.tramadol 0.5mg/kg diluted in 10ml N/s given as iv infusion over 10 minutes
Eligibility Criteria
Sex: | Female |
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Minimum Age: | 18 |
Maximum Age: | 60 |
Age Groups: | Adult |
Healthy Volunteers: | Yes |
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
* 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
Primary Outcomes
More Details
NCT Number: | NCT05311722 |
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Other IDs: | ORehman |
Study URL: | https://clinicaltrials.gov/study/NCT05311722 |
Last updated: Sep 29, 2023