Study to assess time taken for recovery from anesthetic drugs when it is either purely intravenous or purely inhalational or both inhalational and intravenous in fibroadenoma surgery
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/12/060833
- Lead Sponsor
- SRM
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients scheduled to undergo elective excision and biopsy of fibroadenoma
2. ASA I and II patients
3. Females aged 18-45 years
4. Patients with BMI less than 24.9
5. Patients assessed to have MPC I & II
5. Anticipated surgery duration of less than 1 hour
Exclusion Criteria
1. Patients refusal
2. Anticipated difficult airway
3. Patients with history of GERD
4. Patients with history of achalasia
5. Patients with history of oropharyngeal abscess or mass
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method