WHO ICTRP trial
Randomised Controlled Trial of patient-controlled sedation for colonoscopy…
EUCTR2005-003887-48-GB · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2005-003887-48-GB |
|---|---|
| Public title | Randomised Controlled Trial of patient-controlled sedation for colonoscopy: Entonox versus target-controlled infusion of propofol - RCT of patient controlled sedation for colonscopy |
| Scientific title | Randomised Controlled Trial of patient-controlled sedation for colonoscopy: Entonox versus target-controlled infusion of propofol - RCT of patient controlled sedation for colonscopy |
| Primary sponsor | HULL AND EAST YORKSHIRE NHS TRUST |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): yes |
| Countries | United Kingdom |
| Conditions | COLONOSCOPY- NO SPECIFIC MEDICAL CONDITION |
| Interventions | Trade Name: DIPRIVAN 1% Pharmaceutical Form: Injection* Pharmaceutical form of the placebo: Inhalation gas Route of administration of the placebo: Inhalation use Trade Name: ENTONOX Pharmaceutical Form: Inhalation gas |
| Registration date | Oct 25, 2005 |
| Target size | 100 |
| Secondary IDs | R0239 |
| Registry page | clinicaltrialsregister.eu |
At a glance
- No Results available
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: