Health Condition 1: N939- Abnormal uterine and vaginal bleeding, unspecified
Conditions
Interventions
Control Intervention1: PREGABALIN AND PREGABALIN WITH PARACETAMOL. COMPARED WITH CONTROL GROUP.: Group P1. Given pregabalin 150 mg 1 hour prior to surgery
Group P2. Given pregabalin 150 mg with parace
Sponsors
PREMA
Eligibility
Inclusion criteria
Inclusion criteria: 90 patients in 3 groups of 30 each.ASA 1 and 2 Group P1 premedicated with pregabalin 150 mg Group P2 premedicated with pregabalin 150 mg with paracetamol 500 mg Group P3 no premedication given
Exclusion criteria
Exclusion criteria: 1.patient with known allergy to medicine 2.hysterctomy done under general Anaesthesia 3.ASA 3 and above
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the pain after surgery ..to compare post operative pain in controland in study group.Timepoint: Immediate post surgery to first 24 hours | — |
Secondary
| Measure | Time frame |
|---|---|
| Premedication decreases total analgesic doses post op for first 24 hours. To see for any side effects associated with premedicant drugsTimepoint: Pain and sedation score assessed from immediate post op to first 24 hours | — |
Countries
India
Contacts
Public ContactPREMA
IGMC SHIMLA
Outcome results
None listed