Study in which we have compared postoperative pain relief after applying quadratus lumborum block or transversus abdominis plane block using USG in patients undergoing abdominal hysterectomy under general anaesthesia.
- Conditions
- Health Condition 1: N72- Inflammatory disease of cervix uteriHealth Condition 2: N72- Inflammatory disease of cervix uteri
- Registration Number
- CTRI/2022/05/042468
- Lead Sponsor
- JLN medical college Ajmer
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Age group between 18 and 60 years.
Body weight 30 to 80 kg.
Patients belonging to ASA (American Society of Anaesthesiologists) class 1 and 2.
Patients undergoing abdominal hysterectomy of duration 1 to 2 hours in theatre with haemoglobin atleast 9 gm/dl.
Patient free from any associated acute or chronic systemic illness
Patients not willing to participate in the study.
Uncooperative patients.
Patient with chronic pain or on long-term analgesics.
Any known hypersensitivity or contraindication to bupivacaine.
Local pathology at the site of injection or disability limiting the performance of block,(deformity of spine).
Patients receiving beta blockers or cardiac drugs.
History of convulsion, allergy to the drug used, bleeding disorder,severe neurological deficit, thyroid disorder.
Patient with history of respiratory, cardiac, hepatic or renal disease (necessitating classification in ASA Class III or above).
Patients having a history of significant neurological, psychiatric, or neuromuscular disorders.
Pregnant, lactating mothers.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of Number and frequency of postoperative analgesia required in both the <br/ ><br>groups for First 24 hours Postoperatively To assess the effective analgesia by visual <br/ ><br>analog scale (VAS) scoreTimepoint: around 1 year
- Secondary Outcome Measures
Name Time Method To assess and compare the hemodynamic changes . <br/ ><br>To assess and compare the proportion of patients having adverse effects and any other <br/ ><br>complications. <br/ ><br>To acess quality of recovery.Timepoint: around 1 year