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The efficacy of oral pain relief cocktail during panretinal photocoagulation for diabetic retinopathy

The efficacy of oral pain relief cocktail during panretinal photocoagulation for diabetic retinopathy: a randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200915048724N1
Enrollment
30
Registered
2020-10-29
Start date
2020-10-22
Completion date
Unknown
Last updated
2020-11-30

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

Conditions

prolifrative Diabetic retinopathy-non prolifrative Diabetic retinopathy. Diabetes mellitus due to underlying condition with mild nonproliferative diabetic retinopathy with macular edema

Interventions

Intervention 1: Intervention group: At first, 30 patients (60 eyes) are studied, each patient's retin is divided into four parts and in each session one area of each eye is lasered one hour before the

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
51 Years to 69 Years

Inclusion criteria

Inclusion criteria: age: years old proliferative diabetic retinopathy severe non-proliferative diabetic retinopathy no previous laser treatment best corrected visual acuity of 20/200 or better intraocular pressure under 21 mmHg spherical equivalent of ± 5.00 diopters clear media and vitreous severe non-proliferative diabetic retinopathy

Exclusion criteria

Exclusion criteria: previous photocoagulation treatment media opacity such as cataracts, corneal diseases or vitreous hemorrhage unilateral PDR chronic use of analgesics history of any side effects related to pregabalin or novafen Myopic more or equal to 6 Renal Failure

Design outcomes

Primary

MeasureTime frame
Pain in VAS Questionnaire. Timepoint: patient scored the pain sensation immediately after each PRP section using Scott& rsquo s visual analogue scale (VAS). Method of measurement: visual analogue scale (VAS).

Secondary

MeasureTime frame
Blood pressure. Timepoint: Blood pressure were taken by a digital blood pressure monitor 15 min before and immediately after laser treatment. Method of measurement: digital blood pressure monitor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad hossein norouzzade

Shiraz University of Medical Sciences

mkjoharii@gmail.com+98 71 3230 5410

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 12, 2026