comparison of Clonidine and Dexmedetomidine for the duration of Post-operative Pain relief by Femoro-Sciatic Nerve Block in the patients of below knee Surgeries.
Completed
- Conditions
- healthy human volunteers
- Registration Number
- CTRI/2015/10/006328
- Lead Sponsor
- Dr RPGMC Kangra at Tanda
- Brief Summary
to study the effect of adding adjuvent (clonidine and dexmedetomidine) to levo-bupivacaine in prolonging the post operative analgesia in below knee surgeries by femoro-sciatic nerve block.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
- Inclusion criteria – 1.Males and females between the age group 20-60 years.
- 2.ASA class I-II.
- 3.BMI 18.5-39.9. 4.Undergoing surgeries of leg and foot.
Exclusion Criteria
- 1.Patient’s refusal for block.
- 2.History of cardiac, renal or hepatic disease, CNS disorders, neuropathy.
- 3.Chronic treatment with calcium channel blockers.
- 4.Patients having bleeding disorders.
- 5.Hypersensitivity to local anaesthetics.
- 7.Knee surgery.
- 8.Allergic to study drugs.
- 9.Patients with known bradyarrythmia and on beta blocker therapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome measure in this study is the time to first analgesic request. The primary outcome measure in this study is the time to first analgesic request.
- Secondary Outcome Measures
Name Time Method The secondary outcome measures include the number of supplemental analgesic requirements, VAS pain, nausea, patient satisfaction The secondary outcome measures include the number of supplemental analgesic requirements, VAS pain, nausea, patient satisfaction
Trial Locations
- Locations (1)
Dr. RPGMC Kangra at Tanda
🇮🇳Kangra, HIMACHAL PRADESH, India
Dr. RPGMC Kangra at Tanda🇮🇳Kangra, HIMACHAL PRADESH, IndiaBhanu GuptaPrincipal investigator9418016807bhanurpgmc@gmail.com