Actively Recruiting

Age: 21Years - 70Years
All Genders
Healthy Volunteers
ID07368842

Scalp Hair Metabolomics as a Novel Biomarker of Poor Metabolic Health in Individuals With Severe Obesity

Led by Singapore General Hospital · Updated on 2026-02-13

60

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research investigates how body weight and weight-loss surgery affect natural chemicals in scalp hair over time in people with severe obesity. The study also explores how common and severe hair thinning, hair loss, and muscle loss are within the first six months after bariatric surgery. The study will include 30 people with severe obesity scheduled for bariatric surgery and 30 healthy-weight individuals as controls. Participants with severe obesity will be assessed before surgery and again at approximately 4, 12, and 26 weeks after surgery, while healthy controls will be assessed only once at the beginning. Assessments include medical information collection, dietary and quality-of-life surveys, body measurements, scalp photos, hair-pull tests, hair sample collection, and muscle strength tests. Participants will complete various evaluations including grip strength and sit-to-stand speed tests, hair-specific quality-of-life questionnaires, and hair amino acid concentration measurements. The primary outcome is the change in amino acid concentration in hair from enrollment to six months. Secondary outcomes include severity of hair loss and muscle strength changes. The total study duration for those undergoing surgery is six months.

CONDITIONS

Brief Title

Scalp Hair Metabolomics in Severe Obesity

Who Can Participate

Age: 21Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 21 to 70 years
  • Ability to provide informed consent
  • For healthy weight controls: BMI between 18.5 and 24.9 kg/m2
  • For healthy weight controls: No chronic disease
  • For healthy weight controls: No long-term medications
  • For severe obesity group: BMI greater than 32.5 kg/m2
  • For severe obesity group: Scheduled to undergo bariatric surgery
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Any factors likely to limit adherence to the study protocol
  • History of autoimmune or scarring alopecia such as alopecia areata, discoid lupus, or lichen planopilaris

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person) for consent and baseline assessments

Baseline Assessment

Duration - 1 day

Participants undergo baseline assessments including medical information collection, dietary and quality-of-life surveys, body measurements, scalp photos, hair-pull test, hair sample collection, and muscle strength testing.

1 visit (in-person) at enrollment

Post-Surgery Follow-up for Severe Obesity Participants

Duration - Up to 26 ± 4 weeks after surgery

Participants with severe obesity return for follow-up assessments repeating baseline procedures at multiple time points after bariatric surgery.

3 visits (in-person) approximately at 4 ± 2 weeks, 12 ± 4 weeks, and 26 ± 4 weeks post-surgery

Trial Site Locations

Total: 1 location

1

Singapore General Hospital

Singapore, Singapore

Actively Recruiting

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Research Team

H

Hong Chang Tan, MD PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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