Skip to main content
Clinical Trials/NCT05134389
NCT05134389
Completed
Not Applicable

Survey on Gastrointestinal and Nutritional Parameters Among One Anastomosis Gastric Bypass Patients From Different Countries

Assuta Medical Center1 site in 1 country493 target enrollmentMay 18, 2020
ConditionsObesity

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Obesity
Sponsor
Assuta Medical Center
Enrollment
493
Locations
1
Primary Endpoint
Self-reported anthropometric outcomes
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

One Anastomosis Gastric Bypass (OAGB) surgery is a type of bariatric surgery (BS) which is gaining popularity worldwide and is considered to be a simple, safe and effective bariatric procedure in terms of weight loss and comorbidities resolution. However, only limited data exists on the nutritional and gastrointestinal (GI) consequences of this procedure.

This study aimed to gain information on GI and nutritional parameters from a large sample of OAGB patients living in 3 different countries.

Post-OAGB patients across Israel (n=277), Spain (n=105) and Portugal (n=111) were recruited to the study based on the time elapsed since surgery [1-6 months (1-6M), 6-12 months (6-12M) and 1-5 years (1-5Y) post-surgery]. Participants were asked to complete an anonymous survey delivered by SurveyMonkey®️ software which included data on demographics, comorbidities, anthropometrics, GI outcomes and satisfaction with the procedure.

Registry
clinicaltrials.gov
Start Date
May 18, 2020
End Date
November 1, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Shiri Sherf Dagan

Dietitian and Epidemiologist, Principal Investigator

Assuta Medical Center

Eligibility Criteria

Inclusion Criteria

  • age ≥18 years old
  • patients who underwent primary OAGB in the last 5 years

Exclusion Criteria

  • patients who had undergone other bariatric surgery
  • current pregnancy
  • lacked capacity to consent

Outcomes

Primary Outcomes

Self-reported anthropometric outcomes

Time Frame: Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).

Measured by weight changes

Secondary Outcomes

  • A. Self-reported lifestyle outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • A. Self-reported nutritional outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • B. Self-reported nutritional outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • B. Self-reported lifestyle outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • C.Self-reported lifestyle outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • C. Self-reported GI outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • C. Self-reported nutritional outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • A. Self-reported GI outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)
  • B. Self-reported GI outcomes(Only once in accordance to the time group (1-6 months, 6-12 months and 1-5 years post-surgery).)

Study Sites (1)

Loading locations...

Similar Trials