A study to determine the comparative efficacy of three different doses of morphine in the control of pain during knee surgery
Not Applicable
- Conditions
- Health Condition 1: null- ASA grade I â?? II, who are scheduled for diagnostic or therapeutic knee arthroscopic surgery for pain in knee joints/meniscal/ligament repair under Subarachnoid Block.
- Registration Number
- CTRI/2015/02/005490
- Lead Sponsor
- All India Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
Patients of either sex, between age 18 years â?? 60 years, ASA grade I â?? II, who are scheduled for diagnostic or therapeutic knee arthroscopic surgery under Subarachnoid Block and are willing and able to give informed consent will be recruited to the trial.
Exclusion Criteria
ASA Grade III â?? IV
Patients in whom articular drain is left in situ.
Patients in whom Combined Spinal Epidural Analgesia-CSEA was used and epidural catheter is left in situ.
Patients with any contra indication to spinal anesthesia.
5.Patients with any contra indication to Bupivacaine.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative analgesia and Duration of analgesia.Timepoint: 1year
- Secondary Outcome Measures
Name Time Method Postoperative analgesia and Duration of analgesia.Timepoint: 1 year