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Comparison of the oral pregabalin and gabapentin effects as a premedication in pain control after orthopedic surgery on the upper limb.

Comparison of the oral Pregabalin and Gabapentin effects as a premedication in pain control after orthopedic surgery on the upper limb.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211013052759N1
Enrollment
120
Registered
2021-10-20
Start date
2021-11-01
Completion date
Unknown
Last updated
2021-11-01

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

Conditions

Comparison of the effect of gabapantin and oral pregabalin as a prodrug in controlling pain after orthopedic surgery on the upper limb in Imam Khomeini Hospital in Ilam..

Interventions

.Intervention group: 120 patients with random entry conditions will be divided into two groups: pregabalin and gabapentin, so that there will be 60 people in each group. For the pregabalin group (P) o

Sponsors

Ilam University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: Having elective orthopedic surgery on one of the upper limbs with general anesthesia Age range 20_55 years ASA class one and two

Exclusion criteria

Exclusion criteria: Patient or guardian dissatisfaction with participation in the study, severe hemodynamic instability, neurological disease or mental disorders, patients with a history of seizures, acute and chronic kidney disease, patients with a history of pregabalin and gabapentin allergies, alcohol and drug abuse Or a history of chronic analgesia Severe hemodynamic instability Neurological disease or mental disorders Patients with a history of seizures Acute and chronic kidney disease Patient with a history of pregabalin and gabapentin allergies alcohol and drug abuse Or a history of chronic analgesia

Design outcomes

Primary

MeasureTime frame
Pain score in vas questionnaire. Timepoint: Measurement of pain intensity after recovery and 6 and 12 hours after surgery. Method of measurement: Visual analogue scale questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRana Roshanfekr

Ilam University of Medical Sciences

Roshanfekrrana@gmail.com+98 66 4260 8531

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 6, 2026