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Evaluation of post operative pain and stress after cataract surgery after gabapentin pretreatment: a single-blind clinical trial

Evaluation of post operative pain and stress after cataract surgery after gabapentin pretreatment: a single-blind clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211216053424N1
Enrollment
44
Registered
2022-05-14
Start date
2022-06-22
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Cataract Surgery.

Interventions

Intervention 1: Intervention group: Gabapentin 600 mg in the form of two 300 mg capsules will be taken orally 100 minutes before topical anesthesia. Intervention 2: Control group: Two capsules very si

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Age between 18 to 75 years Class 1 and 2 patients based on American society of Anesthesiologist (ASA) Classification (Class 1 includes individuals without underlying disease and Class 2 includes individuals with mild underlying disease) Cataract surgery consent to participate in the study

Exclusion criteria

Exclusion criteria: Emergency surgeries Allergic reaction to Gabapentin BMI more than 35 kg/m2 Psychologic disorders Autoimmune disorders Diabetes mellitus Warfarin use Opium or alcohol addiction History of Malignancy and tumor resection surgery

Design outcomes

Primary

MeasureTime frame
The effect of gabapentin pretreatment on pain severity based on Visual analogue Scale. Timepoint: 15 minutes before surgery, when discharge from recovery, 12 hours and 24 hours after surgery. Method of measurement: Visual analogue Scale.

Secondary

MeasureTime frame
Evaluation of the effect of gabapentin pretreatment on stress level based on GAD-7 after's cataract surgery. Timepoint: 15 minutes before surgery, at the time of discharge from recovery, 12 hours and 24 hours after surgery. Method of measurement: General Anxiety Disorder Assessment (GAD-7).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Soudi

Oroumia University of Medical Sciences

rezasoudi@gmail.com0098334595383

Outcome results

None listed

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