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A study to compare pain relief with pre-operative intravenous paracetamol and intravenous ketorolac after abdominal surgeries.

Comparison of postoperative analgesia by preemptive use of intravenous paracetamol and intravenous ketorolac in patients undergoing laparoscopic surgeries - a randomized control study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/04/024410
Enrollment
48
Registered
2020-04-01
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: K35- Acute appendicitis

Interventions

Intervention1: Ketorolac: Preemtively 30mg Ketorolac in 100 ml NS will be given for post-operative pain relief. Intervention2: Paracetamol: preemtively 1g Paracetamol in 100 ml NS will be given for po

Sponsors

Syed Najeebullah Khadri
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing laparoscopic surgeries. patients deemed fit under ASA-(PS) I &II

Exclusion criteria

Exclusion criteria: Patient refusal patent allergic to ketorolac/paracetamol patients categorized under ASA-(ps)III and above Patients with coagulation disorders Pregnant patients

Design outcomes

Primary

MeasureTime frame
To compare the clinical efficacy of preemptive intravenous paracetamol and intravenous ketorolac in reducing postoperative pain by using the Visual Analogue Score.Timepoint: Pain assessement will be done according to the VAS,in the post-operative period from 2 hours post surgery upto 12 hours at every 2 hour interval.—

Secondary

MeasureTime frame
To determine the need for a rescue drug, effect on hemodynamic parameters and role in early mobilization of patient.Timepoint: Effects on hemodynamic parameters,need for rescue drug,will be recorded during the postoperative,every 2-hour interval monitoring of the patient from 2nd hour to the 12th hour.Any role in early mobilization of the patient would also be determined.—

Countries

India

Contacts

Public ContactSyed Najeebullah Khadri

Shri Sathya Sai Medical College and Research Institute

esenkeyem@gmail.com9786743120

Outcome results

None listed

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