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randomized, prospective, unicentric study to compare H2O versus standard colonoscopy in initially unsedated patients

randomized, prospective, unicentric study to compare H2O versus standard colonoscopy in initially unsedated patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00000431
Enrollment
80
Registered
2010-08-17
Start date
2010-08-22
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

K92.2 D37.4

Interventions

Group 1: H20- group using water to unfold the colon during the colonoscopy Group 2: Control group using air to unfold the colon during the colonoscopy

Sponsors

HSK Wiesbaden
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: all outpatient patients coming for colonoscopy and beeing over the age of 18

Exclusion criteria

Exclusion criteria: pregnancy, coagulopathies ((Quick 50 s, Thrombozyten < 100.000/ml)), post-colon-resection

Design outcomes

Primary

MeasureTime frame
In this study, the main goal is to determine, if a higher rate of colonoscopies without sedation/ with less sedation can be achieved by using warm water instead of air in patients who start colonoscopy without sedation. Each application of sedative medication is documented. In the end the different amounts of sedation can be compared.

Secondary

MeasureTime frame
Ancillary criteria are to investigate the number of required patient turns, the time needed for manual stabilisation of the colon by assistants, demand of sedation(number of BOLI), and patient satisfaction based on the specific technique used (water versus air flow).

Countries

Germany

Contacts

Public ContactInsa Aschmoneit

HSK Wiesbaden

Insa.Aschmoneit@hsk-wiesbaden.de0611432420

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026