ClinicalTrials.gg
CompletedNCT03128645Updated Jul 23, 2024

The Effect of the Abdominal Corset on Colonoscopy

An observational study in Colonoscopy, Complete Colonoscopy and Cecum Intubation Time, sponsored by Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-07-23.

Sponsored by Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital · Observational

Study type
Observational
Model
Other
Time perspective
Prospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

In patients with central obesity, the effect of the abdominal corset on colonoscopy completeness, cecum and ileum intubation time will be investigated.

02

Conditions studied

  • Colonoscopy
  • Complete Colonoscopy
  • Cecum Intubation Time
  • İleum Intubation Time
03

In context

Lead sponsor

Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital is the lead sponsor of 22 studies on the registry; 3 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

The patients who were remotely applying to our clinic and planned for colonoscopy according to ASGE colonoscopy indications.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Above 18 years, Meeting the central obesity criteria Cases where colonoscopy is performed under elective conditions

Exclusion criteria

Exclusion Criteria:

  • In case of emergency, The process is terminated due to bad bowel preparation, Inflammatory bowel disease, Serious arrhythmia, Chronic obstructive pulmonary disease Coronary artery disease The previous abdominal surgery
05

Study design

Observational model
Other
Time perspective
Prospective
Enrollment
100 participants (actual)
Patient registry
No

Groups and cohorts

  • Group 1

    Standard method group

    Device: Abdominal Corset

  • Group 2

    Abdominal corset group

    Device: Abdominal Corset

Interventions

  • DeviceAbdominal Corset

    The patient's colonoscopy procedure in group 2 after randomization will be performed with the abdominal corset.

06

What researchers measure

Primary outcomes

  1. Central Obesity

    BMI ≥ 30 (kg / m2), waist circumference\> 102 cm in men and waist circumference\> 88 cm in women

    Time frame: 01/04/2017- 01/06/2017

  2. Cecum intubation time

    Insertion time of the colonoscope from anus to the cecum (second)

    Time frame: 01/04/2017- 01/06/2017

  3. İleum intubation time

    Insertion time of the colonoscope from cecum to the ileum (second)

    Time frame: 01/04/2017- 01/06/2017

07

Study locations

1 site
  • Kartal Kosuyolu Yuksek Ihtisas Education and Research
    Istanbul, 34000, Turkey (Türkiye)
08

References and documents

Publications

  • Gundes E, Ofkeli O, Uzun O, Senger AS, Polat E, Duman M. Effect of Abdominal Corset on Completion of Colonoscopy and Cecal and Ileocecal Intubation Time in Patients with Central Obesity: A Prospective Randomized Controlled Trial. Ann Ital Chir. 2024;95(4):603-608. doi: 10.62713/aic.3348. PubMed 39186356 ↗

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 23, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03128645
Lead sponsor
Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital
Responsible party
Ebubekir Gündeş (Gastroenterological Surgery, Kartal Kosuyolu Yuksek Ihtisas Education and Research Hospital) — Principal investigator
First posted
Apr 25, 2017
Start date
Apr 1, 2017
Primary completion
Sep 1, 2017
Completion
Dec 15, 2017
Last update
Jul 23, 2024

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jul 2024. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion