Life Style Modification Medical and Surgical Management in Patients With Obesity

NCT ID: NCT04417582

Last Updated: 2020-06-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

RECRUITING

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-01-01

Study Completion Date

2025-12-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

In this is an observational study, obese patients that administed and followed in endocrinology clinic of Marmara University Medical school hospital will follow for clinical and laboratory parameters prospectively for 5 years

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Following available clinical and laboratory parameters will be collected for 5 years Treatment modalities ( life stye modification, medication, bariatric surgery) eating habits quality of life body mass index , blood pressure body fat distribution (impedance measurement) laboratory parameters (serum glucose, OGTT, insülin, lipids,creatinin ,ALT AST,CBC, ferritin calcium, phosphate, Parathormone,25 OH vitamin D, vitamin B12 ,uric acid, albumin, FSH LH testosteron, estrogen ) muscle strength (dynomometer measurement) skin glikolization autoflouresent measurement Bone mineral density mesurements (femur, spine ,forarm)

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Obesity Weight Change, Body Obesity; Endocrine Obesity, Metabolically Benign

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

life syte modification only

obese patients followed with life style modification

bariatric surgey

Intervention Type PROCEDURE

patients undergone bariatric surgery or prescribed antiobesity drugs

medical teatment with antiobesity drugs

patients prescribed antiobesity drugs

bariatric surgey

Intervention Type PROCEDURE

patients undergone bariatric surgery or prescribed antiobesity drugs

bariatric surgery

patients undergone bariatric surgery

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

bariatric surgey

patients undergone bariatric surgery or prescribed antiobesity drugs

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

antiobesity drugs ,liraglutide or orlistat

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Body mass index over 30 kg/m2 age between 18-65 years

Exclusion Criteria

active malignancy pregnancy during involvement period chronic inflamatuar diseases
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Marmara University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Marmara University Medical School Section of Endocrinology and Metabolism

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Dilek Gogas Yavuz, MD

Role: CONTACT

+902166254685

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Dilek Gogas Yavuz, MD

Role: primary

+902166254685

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

09.2019.948

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Vestibular Function in Obesity
NCT07033221 RECRUITING