Capsule Endoscopy in Newly Diagnosed Patients of Celiac Disease
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| ClinicalTrials.gov Identifier: NCT03731806 |
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Recruitment Status :
Withdrawn
(funding for capsule could not be secured)
First Posted : November 6, 2018
Last Update Posted : August 23, 2021
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| Condition or disease |
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| Celiac Disease |
This cross sectional observational study will take place in Medical Unit-II Ruth KM Pfau Civil Hospital Karachi, Pakistan. All newly diagnosed patients of celiac disease between the ages of 8 & 60 years and patients who are currently not on gluten free diet will be included.
Patients having intestinal obstruction, strictures, fistulae, dysphagia, pregnant females will be excluded. Patients having cardiac pacemakers or other implanted electromedical devices and those who are unable to swallow the capsule will also be excluded.
All patients meeting inclusion criteria will be included. Informed consent will be taken from ethics committee. Patients will be provided proper brief information of procedure and confidentiality of the patients will be ensured. Patients will be advised to start clear liquid diet for 24 hours before the procedure. They will be advised to drink Movcol powder 10 sachet in 500ml of water within 20 mins, 12 hours before the procedure. They will be kept nil orally for 08 hours before the procedure. Syrup Infacol (simethicone) 15ml diluted in 50 ml of water will be given 30 mins before the procedure. Patients will be asked to swallow the capsule with 200 ml of water. Patients will be allowed to take food 4 after ingestion of capsule. All patients will be provided with capsule retrieval kit from stool. Patients will be explained to pass any stool after ingestion of capsule till it passed in stool or up to 7 days whichever is earlier. Capsule retrieved will be brought back to investigators for data retrieval from capsule. Reporting will be done by person trained to interpret capsule endoscopy. This will include presence of any pathology, its severity, approximate length and segment of small intestine involved and quality of bowel preparation.
Categorical data will be presented as frequency and percentage, e.g., gender, findings of capsule endoscopy like, bowel preparation, mosaic pattern,ulcers, erythema, telangiectasia etc. Quantitative data will be presented as mean with standard deviation, e.g., age. Involvement of different segments of small intestine (duodenum, jejunum and Ileum) will be documented. Categorical data will be compared on gender by Chi-square test and quantitative data will be analyzed by student's t-test. Significance level will be set at ≤0.05.
| Study Type : | Observational |
| Actual Enrollment : | 0 participants |
| Observational Model: | Case-Only |
| Time Perspective: | Cross-Sectional |
| Official Title: | Extent of Small Bowel Involvement on Capsule Endoscopy in Newly Diagnosed Patients of Celiac Disease |
| Estimated Study Start Date : | April 2019 |
| Estimated Primary Completion Date : | March 2020 |
| Estimated Study Completion Date : | April 2020 |
- Grading of Celiac Disease on Capsule Endoscopy using Bonatto Classification [ Time Frame: 8 hours ]
Bonatto Endoscopic Classification of Celiac
- 0 = Normal
- I = Mostly regular villi, some foci, no mosaic pattern
- II = Agglutinated but visible villi, mosaic pattern
- III = Mosaic pattern, absence of villi
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 8 Years to 60 Years (Child, Adult) |
| Sexes Eligible for Study: | All |
| Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- All newly diagnosed patients of celiac disease between the ages of 8 & 60 years.
- Patients who are currently not on gluten free diet.
Exclusion Criteria:
- Patients having intestinal obstruction, strictures, fistulae, dysphagia will be excluded.
- Pregnant females will be excluded.
- Patients having cardiac pacemakers or other implanted electromedical devices.
- Unable to swallow capsule.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03731806
| Pakistan | |
| Ruth KM Pauf Civil Hospital | |
| Karachi, Sindh, Pakistan, 74000 | |
| Study Chair: | Bader F Zuberi, FCPS | Dow University of Health Sciences |
| Responsible Party: | Tazeen Rasheed, Assistant professor, Dow University of Health Sciences |
| ClinicalTrials.gov Identifier: | NCT03731806 |
| Other Study ID Numbers: |
CAP-CELIAC |
| First Posted: | November 6, 2018 Key Record Dates |
| Last Update Posted: | August 23, 2021 |
| Last Verified: | February 2019 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
| Product Manufactured in and Exported from the U.S.: | No |
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celiac disease capsule endoscopy |
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Celiac Disease Malabsorption Syndromes Intestinal Diseases |
Gastrointestinal Diseases Digestive System Diseases Metabolic Diseases |

