Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. ASA grade I or II fit patients. 2. Patients of child bearing age 3. Patients undergoing lower segment cesarean sections under spinal anaesthesia. 4. Haemodynamically stable patients with all routine investigations within normal limits without any other co-morbidities. 5. Patients who are not on any cardiac related drugs. 6. Availability of written informed consent from concerned patient.
Exclusion criteria
Exclusion criteria: 1. Patients not willing to participate in this study. 2. Patients with ASA physical status III and above physical status. 3. Patients with uncontrolled systemic disorders like neurological, cardiac, metabolic, renal, pulmonary disorders, hepatic disease with coagulation abnormalities etc. 4. Patients having local infection at the site where needle for block was to be inserted 5. Patients with bleeding or coagulation disorders. 6. Patients with known allergies to the study drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To compare the efficacy of dexmedetomidine versus clonidine as an adjuvant to ropivacaine (0.2%) in ultrasound-guided transverse abdominis plane block in patients undergoing lower segment cesarean section on post operative analgesia.Timepoint: The Visual Analogue Scale Score will be recorded 20 minutes after shifting to postoperative recovery room, 1,3,6,12 and 24 hours by an investigator blinded to the group assignment | — |
Secondary
| Measure | Time frame |
|---|---|
| To find out any complications & hemodynamic parameter monitoring of the patient (Pulse rate, Blood Pressure Monitoring)Timepoint: 0, 2, 4, 6, 12 & 24 hours;Sedation scoreTimepoint: The sedation caused by alpha 2 agonist additives will be measured by Ramsay sedation scores at 0,2 ,4, 6, 12, 24 hours | — |
Countries
India
Contacts
Dr D Y Patil Medical College and Hospital, Pimpri, Pune