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Clinical Trial Details — Status: Unknown status

Administrative data

NCT number NCT01491126
Other study ID # SHEBA-11-8951-DC-CTIL
Secondary ID
Status Unknown status
Phase N/A
First received December 11, 2011
Last updated February 24, 2014
Start date January 2012
Est. completion date March 2015

Study information

Verified date February 2014
Source Sheba Medical Center
Contact Dan Carter, MD
Phone 972-3-5302197
Email carterd@zahav.net.il
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The investigators study aim is to determine whether there is a any advantage in starting with upper or lower endoscopy. The main study objective will be the amount of analgesia needed for sustaining the examinee's comfort during the exams. Secondary endpoints will rate of detection of significant pathologies, total time of procedure, examinee's tolerance, time to recovery and examinee's satisfaction.


Recruitment information / eligibility

Status Unknown status
Enrollment 170
Est. completion date March 2015
Est. primary completion date December 2014
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria:

- Age> 18

- Same day bidirectional endoscopy

Exclusion Criteria:

- Prior failed endoscopy.

- Any major complication during previous endoscopy.

- Difficulty in communication with the patients.

- Psychiatric disease or mental retardation.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Sheba medical center Ramat Gan

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (3)

Cho JH, Kim JH, Lee YC, Song SY, Lee SK. Comparison of procedural sequences in same-day bidirectional endoscopy without benzodiazepine and propofol sedation: starting at the bottom or the top. J Gastroenterol Hepatol. 2010 May;25(5):899-904. doi: 10.1111/j.1440-1746.2009.06157.x. — View Citation

Hardwick RH, Armstrong CP. Synchronous upper and lower gastrointestinal endoscopy is an effective method of investigating iron-deficiency anaemia. Br J Surg. 1997 Dec;84(12):1725-8. — View Citation

Urquhart J, Eisen G, Faigel DO, Mattek N, Holub J, Lieberman DA. A closer look at same-day bidirectional endoscopy. Gastrointest Endosc. 2009 Feb;69(2):271-7. doi: 10.1016/j.gie.2008.04.063. Epub 2008 Aug 23. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Dose of mephridine and midazolam Dose of analgestices used in order to achive concious sedation 1 year
Secondary Time to recovery Time to full recovery and release after endoscopies 1 year
Secondary Rate of significant findings Rate of significant findings: colonoscopy: polyps, carcinoma, inflammation, diverticuli, A-V malformations Upper endoscopy: Barret's esophagus, severe esophagitis, gastritis, peptic ulcer disease, polyps and space occupying lesions 1 year
See also
  Status Clinical Trial Phase
Completed NCT03638713 - Comparison of Procedural Sequences in Same-day Painless Bidirectional Endoscopy With Colonoscopic Water Exchange Method N/A
Not yet recruiting NCT04973878 - The Optimal Sequence in Same-day Bidirectional Endoscopy Under Deep Anesthesia. N/A
Recruiting NCT06121609 - ED90 of Remimazolam Anesthesia Induction in Painless Bidirectional Endoscopy in Children Phase 4