Comparison of dexmedetomidine and fentanyl for controlling pain of abdominal surgery

Comparative study of dexmedetomidine and fentanyl for post operative analgesia in patient undergoing abdominal surgery

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2019/07/020446

Enrollment

Registered

2019-07-30

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: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere

Interventions

Intervention1: fentanyl: Loading 1ug/kg within 10 minuts maintenance 0.5ug/kg /hr total 12 hrs intraoperative and post operative Intervention2: Dexemedetomidine: Loading 1ug/kg within 10 minuts mainte

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient undergoing any kind of abdominal surgery 2. ASA grade 1 to 3

Exclusion criteria

Exclusion criteria: 1. Patient refuse to give consent 2. Patients with history of Dementia, severe anaemia (Haematocrist 3. Acute cardiac events. • Patients allergic to drug under study • Patient with history of sleep apnea syndrome, morbidity obese patient. • Duration of surgery extending >4hrs, patient went to postoperative ventilatory support

Design outcomes

Primary

Measure	Time frame
VAS scoreTimepoint: Baseline, 1 to 8 hours at 1 hour interval	—

Secondary

Measure	Time frame
requirement of rescue analgesiaTimepoint: after requirement	—

Countries

India

Contacts

Public ContactProf BB Kushwaha

King George medical university

meetprashant.sachan16@gmail.com9984055934

Outcome results

None listed

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