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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01122004
Other study ID # 8877
Secondary ID
Status Recruiting
Phase Phase 1
First received April 12, 2010
Last updated May 10, 2010

Study information

Verified date March 2010
Source hahid Beheshti University of Medical Sciences
Contact Amir faramarzi, MD
Phone +982122585952
Is FDA regulated No
Health authority Iran: Ethics Committee
Study type Interventional

Clinical Trial Summary

The studied patients will be given randomly one of three following drugs1:Gabapentin2: Pregabalin or placebo for 3 days after Photorefractive keratectomy surgery. The pain will be measured based on visual analog scale(VAS) on the day of operation and on the 3 rd day (morning, evening) and then compared among three groups.


Recruitment information / eligibility

Status Recruiting
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 17 Years and older
Eligibility Inclusion Criteria:

- patients candidate for PRK, 17<age<70

Exclusion Criteria:

- use of any systemic analgesic drugs, drug intolerance, need of systemic or topical administration of NSAIDs or eye drops for allergy and glaucoma, dry eyes, pregnancy, breast feeding

Study Design

Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Pregabalin

Pregabalin


Locations

Country Name City State
Iran, Islamic Republic of Ophthalmic Research Center Tehran

Sponsors (1)

Lead Sponsor Collaborator
hahid Beheshti University of Medical Sciences

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary pain degree based on visual analog scale(VAS)
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