Health Condition 1: N959- Unspecified menopausal and perimenopausal disorder
Conditions
Interventions
Control Intervention1: NIL as its an observational study: NIL as its an observational study
Sponsors
Government Medical College and Hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1. ASA physical status I and II 2. Patients scheduled to undergoes gynaecological surgeries with duration of surgery more than one hour. 3. BMI=20 to =35kg/m².
Exclusion criteria
Exclusion criteria: 1. Refusal by the Patient to participate in the study. 2. Pregnant or Lactating Women. 3. Patient having preoperative hemodynamic instability. 4. Patients having any contraindication for morphine. 5. History of relevant drug allergy 6. History of psychiatric illness, substance abuse 7. Severe cardiovascular(NYHA III / NYHA IV), respiratory(severe obstructive/restrictive pulmonary disease), liver diseases(End Stage Liver Disease) metabolic or neurological disease(Motor defects). 8. Chronic treatment with analgesics 9. Coagulopathy. 10. History of intake of drugs such as imipramine, theophylline, fluvoxamine and antiarrhythmic agents
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To Correlate the preoperative baroreceptor sensitivity with postoperative pain scores in patients scheduled to undergo gynaecological surgeriesTimepoint: 0 hr , 30 mins , 1 hr , 4 hrs , 8 hrs , 12 hrs , 24 hrs | — |
Secondary
| Measure | Time frame |
|---|---|
| 1)To evaluate postoperative pain using visual analogue score (VAS) 2) To calculate cumulative morphine consumption in postoperative periodTimepoint: 0 hr , 30 mins , 1 hr , 4 hrs , 8 hrs , 12 hrs , 24 hrs | — |
Countries
India
Contacts
Public ContactDr Richa Saroa
Government Medical College and Hospital, sector 32B, Chandigarh.
Outcome results
None listed