Comparison Of Effects Of Pregabalin and Clonidine On Pain, Sedation and Recovery From General Anesthesia After Laparoscopic Hysterectomy
Not Applicable
Completed
- Conditions
- Health Condition 1: N95- Menopausal and other perimenopausal disorders
- Registration Number
- CTRI/2020/12/029541
- Lead Sponsor
- Institute of Medical Sciences And SUM Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
1. Patients belonging to ASA Grade-I status
2. Patients posted for elective laparoscopic hysterectomy
Exclusion Criteria
1. Refusal of the patient to participate in the study
2. Patients belonging to ASA Grade II/III/IV status
3. Any known allergies to Clonidine or Pregabalin
4. Patients with any chronic pain syndrome under treatment with any GABAergic drugs
5. Patients in whom laparoscopy was converted to laparotomy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Degree of pain assessed by 10-point Visual Analogue Scale (VAS)Timepoint: At baseline, 1, 2, 4, 6, 12 and 24 hours respectively.
- Secondary Outcome Measures
Name Time Method Degree of Sedation measured by Ramsay Sedation Scale(RSS)Timepoint: At baseline, 6, 12 and 24 hours respectively.;Recovery measured using Modified Aldrete scoreTimepoint: Before discharge to ward from the recovery room