Two Different Doses Of Epidural Tramadol For Postoperative Analgesia In Patients Undergoing Upper Abdominal Surgery

A Comparative Study to Evaluate Two Different Doses of Epidural Tramadol for Postoperative Analgesia in Patients Undergoing Upper Abdominal Surgery - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/01/079183

Enrollment

Registered

2025-01-21

Start date

Unknown

Completion date

Unknown

Last updated

2025-02-03

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

Conditions

Health Condition 1: K00-K95- Diseases of the digestive system

Interventions

Intervention1: Inj. Tramadol 1mg/kg body weight: Inj. Tramadol 1mg/kg body weight, route of administration - Epidural catheter, dose repeated when NRS score more than or equal to 4, till 24hrs Control

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I and II, Patients scheduled for upper abdominal surgeries, Elective surgeries

Exclusion criteria

Exclusion criteria: ASA grade III, IV and V Age less than 18 and more than 60 years Patients refusing to give consent Patients who are pregnant or lactating Patients having any bleeding diathesis or are on anticoagulant therapy

Design outcomes

Primary

Measure	Time frame
1.To compare duration of analgesia in both groups 2.To study postoperative pain relief in both groups (by numerical rating scale for pain intensity)Timepoint: 24 hours postoperative	—

Secondary

Measure	Time frame
1.To compare postoperative complication in both groups. 2.Postoperative hemodynamic parameters in both groups. Timepoint: 24 hours postoperative	—

Countries

India

Contacts

Public ContactDr Nilesh Solanki

B. J. Medical college Ahmedabad

nmscbaps@gmail.com9998991716

Outcome results

None listed

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