Actively Recruiting

Phase Not Applicable
Age: 25Years - 65Years
All Genders
NCT07495787

Magnetic Compression Anastomosis Procedure for Partial Jejunoileal Anastomosis: Assessing the Viability of an Innovative Metabolic Approach

Led by iIDEAS Group Holdings Limited · Updated on 2026-03-27

5

Participants Needed

1

Research Sites

75 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

English, Hindi and Gujarati

CONDITIONS

Official Title

Magnetic Compression Anastomosis Procedure for Partial Jejunoileal Anastomosis: Assessing the Viability of an Innovative Metabolic Approach

Who Can Participate

Age: 25Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Willing and able to give informed consent
  • Male or female aged 25 to 65 years
  • Body Mass Index (BMI) of 25 to less than 50
  • Clinical diagnosis of type 2 diabetes mellitus by plasma glucose or A1C criteria
  • Glycated Hemoglobin (HbA1c) between 7.5% and less than 10.5% within the past 3 months
  • Currently taking oral combination therapy for type 2 diabetes
  • At least 12 months of experience with diabetes self-management and support
Not Eligible

You will not qualify if you...

  • Pregnancy, breastfeeding, or planning pregnancy within 9-12 months
  • Mentally or physically disabled, prisoner, or vulnerable individual
  • Current participation in another research study or participation within past 30 days
  • Current use of injected Glucagon Like Peptide 1 (GLP1) therapy
  • American Society of Anesthesiologists (ASA) level 4 or higher
  • History of severe hypoglycemia or hypoglycemia unawareness
  • Evidence of type 1 diabetes or pancreatic exhaustion
  • Unusual or challenging gastrointestinal anatomy or history of small bowel surgery
  • Active or untreated H. pylori infection
  • History of pancreatitis, active hepatitis, or active liver disease
  • Symptomatic gallstones, kidney stones, or acute cholecystitis
  • History of coagulopathy or upper gastrointestinal bleeding conditions
  • Use of anticoagulation or P2Y12 inhibitors that cannot be stopped around procedure
  • Serious diabetes complications including coronary artery disease or diabetic retinopathy
  • Use of corticosteroids, GI motility drugs, or weight loss medications
  • Persistent anemia (hemoglobin less than 10 g/dL)
  • Severe kidney impairment (eGFR or MDRD less than 30 ml/min/1.73m2)
  • Active systemic infection
  • Chemotherapy within 9 months, recent abdominal radiation, or active malignancy within 5 years
  • Active substance abuse or alcoholism
  • Known sensitivities to medications used in the procedure
  • Other serological markers associated with poor outcomes

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

AB Plus Speciality Hospital

Ahmedabad, Gujarat, India, 380054

Actively Recruiting

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Research Team

P

Purvi A Chavda, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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