PVB VERSUS EPIDURAL FOR PAIN RELIEF IN PNEUMECTOMY PATIENTS
Not Applicable
Recruiting
- Conditions
- Analgesic efficacy of regional block in geriatric patients with bronchiectasis.Bronchiectasis
- Registration Number
- IRCT20230812059125N1
- Lead Sponsor
- CMH Rwp
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 106
Inclusion Criteria
Included all ASA-II and III patients between ages 60-70 years presenting in the thoracic surgical department for partial pneumectomy for bronchiectasis
Exclusion Criteria
Major cardiac or respiratory disease
Low ejection fraction
Infection at block site
Coagulation disorders
Allergic to bupivacaine or nalbuphine
Unwilling to be included in the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary variables measured were per-operative analgesia requirement, patient satisfaction for pain relief 24 hours after surgery and 24- hour total dose of analgesia needed after the block. Timepoint: Pain relief and total analgesia needed after the block intervention for 24 hours. Method of measurement: Total dose of analgesia needed by adding doses from the proforma and pain score by the stadard visual analog scale.
- Secondary Outcome Measures
Name Time Method Secondary variables observed were hypotension, nausea, shivering and respiratory depression. Timepoint: For 24 hours after block administration. Method of measurement: Frequency of symptoms as noted by the resident anesthetist on duty in the high dependency unit.