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Comparison of preventive effects of diclofenac vs ibuprofen on succinylcholine induced pain in precurarized patients

Comparison of prophylactic effects of diclofenac vs ibuprofen on succinylcholine induced myalgia in precurarized patients. Randomized, controlled, double blinded study - nil

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/06/068750
Enrollment
60
Registered
2024-06-12
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: iv diclofenac : iv diclofenac Patients of this group will receive inj diclofenac sodium 75 mg in 100 ml NS as infusion over a period of 10 mins before induction of anesthesia and atracu

Sponsors

Sharda Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients scheduled for any elective surgery under general anesthesia with endotracheal intubation under succinylcholine. 2.ASA class I and II 3.Age 18-60 years 4.Both genders

Exclusion criteria

Exclusion criteria: 1. Patients already taking steroids, analgesics, antiemetic, and sedatives preoperatively for any clinical purpose. 2. Patients with past history of chronic pain. 3. Patients having history of endocrine, cardiovascular, renal or CNS disease. 4. Patients allergic to study drugs. 5. Contraindication of succinylcholine e.g. High potassium level, extensive burn or soft tissue injury. 6.BMI more than 30

Design outcomes

Primary

MeasureTime frame
To compare the effects of premedication with two drugs (diclofenac vs ibuprofen) on succinylcholine induced postoperative myalgia in precurarized patients.Timepoint: 72 hrs

Secondary

MeasureTime frame
a) To observe and compare the grades of fasciculations. b) To compare the changes in the levels of serum creatinekinase c) To assess the relationship of fasciculations with serum creatinekinase and myalgia d) To compare the hemodynamic parameters (HR, SBP, DBP, MAP) perioperatively in four groups Timepoint: 72 hrs

Countries

India

Contacts

Public ContactDr HIYA CHATUEVDI

School of Medical Sciences and Research

mahendra.kumar@sharda.ac.in8287188449

Outcome results

None listed

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