PCOS-01: Ovary Syndrome for Efficient Diagnosis and Targeted Therapy

Sponsor
Asian Institute of Gastroenterology, India (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06102629
Collaborator
(none)
200
1
2
36.3
5.5

Study Details

Study Description

Brief Summary

OBJECTIVES:
  1. Analysis of DNA methyl transferases (DNMT1, DNMT3A and DNMT3B) and Histone deacetylases (HDAC 1,2,3 and SIRTs) polymorphisms (Somatic and germ line variations).

  2. Analysis of differential mRNA and protein expression of epigenetic markers in ovarian tissues obtained from PCOS patients.

  3. miRNA regulated epigenetic mechanisms in PCOS

  4. Epigenetic regulation of endocrine genes in PCOS

DESIGN : A Case Control study.Sample size:200

Condition or Disease Intervention/Treatment Phase
  • Procedure: laparoscopy / laparotomy
  • Other: NO INTERVENTION
N/A

Detailed Description

  1. We will take both blood and ovarian tissue samples used to diagnosis.

  2. We will take approximately 3 ml of blood which will be used from the blood sample collected for routine preoperative tests (surgical profile) before their planned surgery or for disease evaluation.

  3. Small tissue samples (from ovary) will be taken from the tissue which is surgically excised as a part of treatment.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
This is a Case control study with two parallel groupsThis is a Case control study with two parallel groups
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Understanding the Epigenetic Mechanisms in the Pathophysiology of Polycystic Ovary Syndrome for Efficient Diagnosis and Targeted Therapy
Anticipated Study Start Date :
Nov 5, 2023
Anticipated Primary Completion Date :
Nov 15, 2026
Anticipated Study Completion Date :
Nov 15, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: 100 women undergoing surgery (laparoscopy / laparotomy) with presumed diagnosis of PCOS (

We will take both blood and ovarian tissue samples used to diagnosis. We will take approximately 3 ml of blood which will be used from the blood sample collected for routine preoperative tests (surgical profile) before their planned surgery or for disease evaluation. Small tissue samples (from ovary) will be taken from the tissue which is surgically excised as a part of treatment.

Procedure: laparoscopy / laparotomy
We will take both blood and ovarian tissue samples used to diagnosis. We will take approximately 3 ml of blood which will be used from the blood sample collected for routine preoperative tests (surgical profile) before their planned surgery or for disease evaluation. Small tissue samples (from ovary) will be taken from the tissue which is surgically excised as a part of treatment.

Other: NO INTERVENTION
.We will take both blood and ovarian tissue samples used to diagnosis. 2.We will take approximately 3 ml of blood which will be used from the blood sample collected for routine preoperative tests (surgical profile) before their planned surgery or for disease evaluation. 3. Small tissue samples (from ovary) will be taken from the tissue which is surgically excised as a part of treatment.

No Intervention: 100 women undergoing surgery for gynaecological disorder

We will take both blood and ovarian tissue samples used to diagnosis. We will take approximately 3 ml of blood which will be used from the blood sample collected for routine preoperative tests (surgical profile) before their planned surgery or for disease evaluation. Small tissue samples (from ovary) will be taken from the tissue which is surgically excised as a part of treatment.

Outcome Measures

Primary Outcome Measures

  1. Evaluate the Analysis of DNA methyl transferases [3 YEARS]

    DNA will be extracted as per the protocol followed routinely in our lab from blood and ovarian tissues.

  2. Evaluate the Analysis of differential mRNA and protein expression of epigenetic markers in ovarian tissues [3 YEARS]

    Total RNA from ovarian tissue will be extracted using TRIzol reagent according to the manufacturer's instructions (Invitrogen Life Technologies) and reverse transcribed in the presence of random hexamers. Quantitative real-time PCR reactions will be carried out in an ABI 7000 Thermal Cycler (Applied Biosystems) to analyse the expression of epigenetic markers including the androgen regulated miRNAs and their downstream targets.

Secondary Outcome Measures

  1. understand miRNA regulated epigenetic mechanisms [3 YEARS]

    The present study would investigate the expression pattern of DNMTs, HDACs, miRNAs and their downstream targets in Ovarian tissues (samples of normal adult ovaries and polycystic ovaries) by western blot and immunohistochemical analysis (IHC).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • All the subjects would be of Indian origin (controls ~100, cases ~100). They would be in their reproductive age (18-45 yrs). Rotterdam consensus would be used to diagnose PCOS and cases will be selected based on it.

Criteria for the diagnosis of PCOS would include oligo-ovulation cycles longer than 35 days or less than 26 days, elevated free testosterone levels (0.5 ng/dl; the cutof level for free testosterone level was the mean±2 SD according to normal levels in controls), oligomenorrhea or amenorrhea.

A Ferriman-Gallwey (FG) score of≥7 would be taken as indicator for the presence of hirsutism. In accordance with the above criteria, polycystic ovary morphology would be determined by transvaginal ultrasonography, which defines PCOS as the presence of 12 or more small (2-9 mm) follicles in each ovary.

Control subjects would have no signs of menstrual dysfunction and their androgen levels should be within the normal range, with normal glucose tolerance, and no family history of hirsutism, type 2 diabetes mellitus, and infertility.

Exclusion Criteria:
  • Women with other causes of hyperandrogenism such as hyperprolactinemia, androgen-secreting tumors, Cushing syndrome and nonclassic congenital hyperplasia would be excluded from this study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Dr. Shraddha Ramchandani Hyderabad Telangana India 500082

Sponsors and Collaborators

  • Asian Institute of Gastroenterology, India

Investigators

  • Principal Investigator: Shraddha Ramchandani, AIG HOSPITALS

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Asian Institute of Gastroenterology, India
ClinicalTrials.gov Identifier:
NCT06102629
Other Study ID Numbers:
  • PCOS-01
First Posted:
Oct 26, 2023
Last Update Posted:
Oct 26, 2023
Last Verified:
Oct 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 26, 2023