Trial Outcomes & Findings for Comparison of Oral Gabapentin and Pregabalin in Postoperative Pain Control After Photorefractive Keratectomy (NCT NCT00954187)

NCT ID: NCT00954187

Last Updated: 2017-01-09

Results Overview

No data was collected or analyzed. No study procedures were performed.

Recruitment status

TERMINATED

Study phase

NA

Target enrollment

8 participants

Primary outcome timeframe

one month

Results posted on

2017-01-09

Participant Flow

Participant milestones

Participant milestones
Measure
Gabapentin
Neurontin Gabapentin: Gabapentin - 300 mg three times a day starting two hours prior to surgery and will continue for a total of four days
Pregabalin
Lyrica pregabalin: 50 mg PO TID
Overall Study
STARTED
0
0
Overall Study
COMPLETED
0
0
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Comparison of Oral Gabapentin and Pregabalin in Postoperative Pain Control After Photorefractive Keratectomy

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Gabapentin
Neurontin Gabapentin: Gabapentin - 300 mg three times a day starting two hours prior to surgery and will continue for a total of four days
Pregabalin
Lyrica pregabalin: 50 mg PO TID
Total
Total of all reporting groups
Gender
Female
0
n=5 Participants
Gender
Male
0
n=5 Participants

PRIMARY outcome

Timeframe: one month

Population: No subjects were assigned treatment and no study procedures were performed

No data was collected or analyzed. No study procedures were performed.

Outcome measures

Outcome data not reported

Adverse Events

Gabapentin

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Pregabalin

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Julio Narvaez, MD

Loma Linda University

Phone: 9095589408

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place