Comparing two drugs as adjuvants to local anaesthetic in patients of carcinoma cervix undergoing brachytherapy procedure
Not Applicable
- Conditions
- Health Condition 1: C539- Malignant neoplasm of cervix uteri, unspecified
- Registration Number
- CTRI/2022/05/042677
- Lead Sponsor
- Homi Bhabha Cancer Hospital Research Centre Punjab
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1)Patients of carcinoma cervix posted for intracavitary brachytherapy
2)Written informed consent
Exclusion Criteria
1)Refused consent for spinal anaesthesia
2)Patients who need admission overnight
3)Any contraindications to spinal anaesthesia (including coagulopathy, low absolute neutrophil count, allergic to local anaesthetic)
4)Patients with raised intracranial pressure, peripheral neuropathy, demyelinating central nervous system disorders, local sepsis were excluded
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparing the absolute duration of spinal analgesia among the two groups.Timepoint: Over 12 hours post-spinal anaesthesia.
- Secondary Outcome Measures
Name Time Method 1. VAS Pain Scores <br/ ><br>2. Quality of spinal anaesthesia <br/ ><br>3. Sedation Score <br/ ><br>4. Time to achieve hospital discharge criteria <br/ ><br>5. Patient Satisfaction ScoreTimepoint: 1.5-15 minutes during procedure after that every 30 minutes <br/ ><br>2. At the end of procedure <br/ ><br>3. 5-15 minutes during procedure after that every 30 minutes <br/ ><br>4. Every 30 minutes post procedure <br/ ><br>5. After 12 hrs post spinal anaesthesia.