Assessment of Serum Asprosin Level in Male Patients With Acne Vulgaris

Sponsor
Sohag University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05471388
Collaborator
(none)
72
1
2
6
11.9

Study Details

Study Description

Brief Summary

Subject of interest is to evaluate serum level of asprosin in male patients with acne vulgaris, demonstrate the relation between acne vulgaris severity and level of asprosin in these patients & the relation between metabolic syndrome in acne vulgaris and level of asprosin.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: serum asprosin
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
72 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Assessment of Serum Asprosin Level in Male Patients With Acne Vulgaris
Anticipated Study Start Date :
Jul 18, 2022
Anticipated Primary Completion Date :
Jan 18, 2023
Anticipated Study Completion Date :
Jan 18, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: case

Diagnostic Test: serum asprosin
assessment of serum asprosin by a commercially available double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) kit.

Active Comparator: control

Diagnostic Test: serum asprosin
assessment of serum asprosin by a commercially available double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) kit.

Outcome Measures

Primary Outcome Measures

  1. Assess serum asprosin level in male patients with acne vulgaris. [6 months]

    Assess serum asprosin level in male patients with acne vulgaris.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Acne vulgaris male patients (>18 years) will be included.
Exclusion Criteria:
  • Age <18 years.

  • Females.

  • Patients with other inflammatory skin disorders.

  • Patients with associated systemic diseases.

  • Current or previous treatment with isotretinoin in the last 3 month ,anti-inflammatory drugs, systemic antibiotics, androgen or anti androgen therapy, and steroid therapy).

  • Patients known on treatment of diabetes, hypertension and dyslipidemia.

  • Athletes.

  • Patient refusal.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sohag University Hospital Sohag Egypt

Sponsors and Collaborators

  • Sohag University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Esraa Abdel-Azeem Hamoda, resident doctor at Dematology, Venereology and Andrology department at Sohag University Hospital, Sohag University
ClinicalTrials.gov Identifier:
NCT05471388
Other Study ID Numbers:
  • Soh-Med-22-07-06
First Posted:
Jul 22, 2022
Last Update Posted:
Jul 22, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Esraa Abdel-Azeem Hamoda, resident doctor at Dematology, Venereology and Andrology department at Sohag University Hospital, Sohag University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 22, 2022