Skip to content

Post operative pain comparison in patients undergoing elective laparoscopic surgery who is receving fentanyl and the patients who is receiving dexmedetomidine

Comparison of opioid free versus opioid based anaesthesia on postoperative pain intensity for laparoscopic surgeries, a randomised prospective double blinded study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/01/030301
Enrollment
70
Registered
2021-01-07
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K353- Acute appendicitis with localizedperitonitis Health Condition 2: K810- Acute cholecystitis Health Condition 3: K800- Calculus of gallbladder with acutecholecystitis Health Condition 4: K801- Calculus of gallbladder with othercholecystitis Health Condition 5: K802- Calculus of gallbladder without cholecystitis Health Condition 6: N921- Excessive and frequent menstruation with irregular cycle Health Condition 7: N920- Excessive and frequent menstruation with regular cycle

Interventions

Intervention1: DEXMEDETOMIDINE, KETAMINE: Inj Dexmedetomidine infusion 1mcg/kg/body weight diluted to 100ml NS over 10-15 minutes before induction along with Inj Ketamine 25mg to patients posted for e

Sponsors

JSS MEDICAL COLLEGE AND HOSPITAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of ASA physical status class 1 and 2 aged 20-60 years undergoing elective laparoscopic surgeries lasting for <2 hours

Exclusion criteria

Exclusion criteria: Pregnant, breast feeding women, hepatic, renal or cardiac insufficiency, psychiatric disease, allergy or contraindicated to study drugs, BMI >30, Obstructive sleep apnoea syndrome.

Design outcomes

Primary

MeasureTime frame
Amount of post-operative pain intensity in terms of visual analogue score (VAS) and rescue analgesics requirementsTimepoint: starting of general anaesthesia till twenty four hours after completion of surgery.

Secondary

MeasureTime frame
1. Assessment of intraoperative haemodynamic stability. 2. Post-operative recovery status. 3. Post-operative sedation in terms of Ramsay-sedation scoring system. 4. Incidence of post-operative nausea and vomiting. Timepoint: starting of general anaesthesia till twenty four hours after completion of surgery.

Countries

India

Contacts

Public ContactDr GURUDATT C L

jss medical college and hospital, mysuru

dattguru55@gmail.com9845312311

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026