Trial Outcomes & Findings for The Effects of the Water Drinking Test on Intraocular Pressure (NCT NCT01507584)

NCT ID: NCT01507584

Last Updated: 2019-09-11

Results Overview

Assess IOP patterns between day and night time and changes after the WDT.

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

23 participants

Primary outcome timeframe

24-hour

Results posted on

2019-09-11

Participant Flow

The PI has left the institution and the study data can not be located. Multiple attempts where made to reach the study team, so there are no results to report.

Participant milestones

Participant milestones
Measure
ALL PARTICIPANTS
Overall Study
STARTED
0
Overall Study
COMPLETED
0
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

The Effects of the Water Drinking Test on Intraocular Pressure

Baseline characteristics by cohort

Baseline data not reported

PRIMARY outcome

Timeframe: 24-hour

Population: The PI has left the institution and the study data can not be located. Multiple attempts where made to reach the study team, so there are no results to report.

Assess IOP patterns between day and night time and changes after the WDT.

Outcome measures

Outcome data not reported

PRIMARY outcome

Timeframe: 24-hours

Population: The PI has left the institution and the study data can not be located. Multiple attempts where made to reach the study team, so there are no results to report.

IOP monitoring sessions will be carried out in ambulatory mode at 4 week intervals (plus/minus 7 days)

Outcome measures

Outcome data not reported

SECONDARY outcome

Timeframe: 24-hours

Population: The PI has left the institution and the study data can not be located. Multiple attempts where made to reach the study team, so there are no results to report.

appearance of any device- or non-device-related ocular adverse events

Outcome measures

Outcome data not reported

Adverse Events

ALL PARTICIPANTS

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

Eunice Williams-Steppe

ucsdmed

Phone: 8588221133

Results disclosure agreements

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