Status unknownNCT00563069Updated Jul 7, 2010

Premedication With Oral Midazolam in Patients Undergoing Rigid Cystoscopy: A Randomized, Double-blind, Placebo-controlled Trial

An interventional study of Midazolam in Cystoscopy, sponsored by Hospital Authority, Hong Kong. Status unknown at 1 site in China. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2010-07-07.

Sponsored by Hospital Authority, Hong Kong · Not applicable, Interventional, and Prevention

The sponsor has not verified this record recently (last verified Jul 2010), so the status shown — last known as Recruiting — may be out of date.

Phase: Not applicable
Study type: Interventional
Enrollment: 120
Allocation: Randomized
Ages: 18 Years to 80 Years
Sex: All

Study summary

To investigate the efficacy of oral midazolam for patients undergoing rigid cystoscopy in:

relieving patient's anxiety and improving satisfaction
reducing procedure-related pain
facilitating the diagnostic and therapeutic interventions during rigid cystoscopy

Conditions studied

Cystoscopy

Keywords

diagnostic and therapeutic rigid cystoscopy

In context

Lead sponsor

Hospital Authority, Hong Kong is the lead sponsor of 73 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

Who can participate

Ages eligible: 18 Years to 80 Years
Sexes eligible: All

Inclusion criteria

Elective rigid cystoscopy
Either diagnostic or therapeutic
Age between 18 to 80

Exclusion criteria

Exclusion Criteria:

Patients with allergy to midazolam or other benzodiazepine groups
Pregnancy
Emergency rigid cystoscopy
ASA class 3 or above
Patients on psychiatric medications
Alcoholics

Study design

Phase: Not applicable
Primary purpose: Prevention
Allocation: Randomized
Intervention model: Single group
Masking: Double
Enrollment: 120 participants (estimated)

Interventions

DrugMidazolam

What researchers measure

Primary outcomes

Pain score during the procedure as assessed by visual analog scale

Secondary outcomes

Patient's satisfaction
Patient's willingness to repeat the procedure
Patient's cooperativeness during the procedure as assessed by surgeons

Study locations

1 of 1 sites recruiting

Department of Surgery, Prince of Wales Hospital
Hong Kong, China
- Wilfred LM Mui, Dr · Sub investigator
- Chi Fai Ng, Dr · Sub investigator
- Michael CW Cheng, Dr · Sub investigator
- Shu Yin Chan, Dr · Sub investigator
Recruiting

Updates

Tracking since Sep 25, 2026

No changes since tracking began. The registry record was last updated on Jul 7, 2010, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT00563069
Lead sponsor: Hospital Authority, Hong Kong
Collaborators: Chinese University of Hong Kong
First posted: Nov 26, 2007
Start date: Sep 2005
Completion: Dec 2006 (estimated)
Last update: Jul 7, 2010

Study contacts

Shirley YW Liu, Dr

Contact

liu_yws@yahoo.com.hk

(852) 2632 2625

Shirley YW Liu, Dr

principal investigator · Department of Surgery, Prince of Wales Hospital/ The Chinese Univerisity of Hong Kong

View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2010. You cannot join it, but the record below documents what was studied.

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Discussion

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