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CTRI Number  CTRI/2025/01/079591 [Registered on: 27/01/2025] Trial Registered Prospectively
Last Modified On: 25/07/2025
Post Graduate Thesis  Yes 
Type of Trial  Interventional 
Type of Study   Drug 
Study Design  Randomized, Parallel Group, Active Controlled Trial 
Public Title of Study   Comparison of Dienogest versus Freedase in Endometriosis associated pain. 
Scientific Title of Study   Comparison of Dienogest alone versus Dienogest and Ethinyl Estradiol for Endometriosis Pain Relief: an open label Randomized controlled Trial. 
Trial Acronym  NIL 
Secondary IDs if Any  
Secondary ID  Identifier 
NIL  NIL 
 
Details of Principal Investigator or overall Trial Coordinator (multi-center study)  
Name  JENCY S 
Designation  Post Graduate Registrar [Obstetrics and Gynaecology] 
Affiliation  Christian Medical College, Vellore. 
Address  Unit II, Department of Obstetrics and Gynaecology, Christian Medical College, Vellore.

Vellore
TAMIL NADU
632004
India 
Phone  7299850448  
Fax    
Email  francilinjency@gmail.com  
 
Details of Contact Person
Scientific Query
 
Name  DR PUSHPLATA KUMARI 
Designation  Associate Professor [Obstetrics and Gynaecology] 
Affiliation  Christian Medical College, Vellore. 
Address  Unit II, Department of Obstetrics and Gynaecology, Christian Medical College, Vellore.

Vellore
TAMIL NADU
632004
India 
Phone  9500359929  
Fax    
Email  manpushp05@gmail.com  
 
Details of Contact Person
Public Query
 
Name  JENCY S 
Designation  Post Graduate Registrar [Obstetrics and Gynaecology] 
Affiliation  Christian Medical College, Vellore. 
Address  Unit II, Department of Obstetrics and Gynaecology, Christian Medical College, Vellore.

Vellore
TAMIL NADU
632004
India 
Phone  7299850448  
Fax    
Email  francilinjency@gmail.com  
 
Source of Monetary or Material Support  
Fluid Research Grant, Institutional Review Board, Christian Medical College, Vellore, TamilNadu - 632004, India. 
 
Primary Sponsor  
Name  Institutional Review Board and Ethics Committee, Christian Medical College, Vellore 
Address  Institutional Review Board(IRB), Bagayam campus, Office of Research, 1st Floor, Carman Block, Bagayam, Vellore - 632002. 
Type of Sponsor  Private medical college 
 
Details of Secondary Sponsor  
Name  Address 
NIL  NIL 
 
Countries of Recruitment     India  
Sites of Study  
No of Sites = 1  
Name of Principal Investigator  Name of Site  Site Address  Phone/Fax/Email 
Dr Jency S  Christian Medical College  OPD Department, Department of Obstetric and Gynaecology
Vellore
TAMIL NADU 
7299850448

francilinjency@gmail.com 
 
Details of Ethics Committee  
No of Ethics Committees= 1  
Name of Committee  Approval Status 
Institutional Review Board and Ethics Committee, Christian Medical College, Vellore.  Approved 
 
Regulatory Clearance Status from DCGI  
Status 
Not Applicable 
 
Health Condition / Problems Studied  
Health Type  Condition 
Patients  (1) ICD-10 Condition: N809||Endometriosis, unspecified,  
 
Intervention / Comparator Agent  
Type  Name  Details 
Comparator Agent  Combination of Dienogest and Ethinyl estradiol  Oral tablet - Combination of Dienogest(2mg) and Ethinyl estradiol(30mcg) once daily for 84 days(12 weeks) + 84 days(12 weeks). 
Intervention  Tab.Dienogest  Oral Dienogest 2mg once dailuy for 84 days(12 weeks) + 84 days(12 weeks) 
 
Inclusion Criteria  
Age From  20.00 Year(s)
Age To  45.00 Year(s)
Gender  Female 
Details  1. Clinically, Histologically or Radiologically diagnosed endometriosis.
2. Presence of Pain symptoms associated with endometriosis like Dysmenorrhea, Dyspareunia or non-cyclical chronic pelvic pain.
3. Baseline VAS score for pain of more than or equal to 4 at time of enrollment. 
 
ExclusionCriteria 
Details  1. Current user of hormonal therapy or used within 2 months.
2. Presence of pregnancy, lactation or planning to conceive.
3. Previous history of failed improvement with the study medication.
4. History of drug reaction to steroid hormones or COC or Dienogest.
5. Contraindication for Estrogen and or Progesterone.
6. Planned for surgical treatment for endometriosis or other medical therapy.
7. Pain due to causes other than endometriosis.
8. Not willing to participate or not willing for follow up.  
 
Method of Generating Random Sequence   Computer generated randomization 
Method of Concealment   Pre-numbered or coded identical Containers 
Blinding/Masking   Open Label 
Primary Outcome  
Outcome  TimePoints 
Change in the endometriosis associated pain assessed by Visual Analogue Score (VAS score) from the baseline.  Baseline, 12 weeks and 24 weeks  
 
Secondary Outcome  
Outcome  TimePoints 
Change in the Self-reported Pain symptoms (chronic pelvic pain, dysmenorrhea & dyspareunia) assessed by the Biberoglu & Behrman (B&B) scale.
Improvement in the Health-related quality of life (HRQoL) after starting the treatment assessed by Endometriosis Health Profile - 30 (EHP-30) questionnaire
Change in the mean diameter of ovarian endometrioma
Comparison of safety & tolerability of either treatment. 
Baseline, 12 weeks & 24 weeks 
 
Target Sample Size   Total Sample Size="110"
Sample Size from India="110" 
Final Enrollment numbers achieved (Total)= "Applicable only for Completed/Terminated trials"
Final Enrollment numbers achieved (India)="Applicable only for Completed/Terminated trials" 
Phase of Trial   Phase 3 
Date of First Enrollment (India)   01/02/2025 
Date of Study Completion (India) Applicable only for Completed/Terminated trials 
Date of First Enrollment (Global)  Date Missing 
Date of Study Completion (Global) Applicable only for Completed/Terminated trials 
Estimated Duration of Trial   Years="3"
Months="0"
Days="0" 
Recruitment Status of Trial (Global)
Modification(s)  
Not Applicable 
Recruitment Status of Trial (India)  Open to Recruitment 
Publication Details   N/A 
Individual Participant Data (IPD) Sharing Statement

Will individual participant data (IPD) be shared publicly (including data dictionaries)?  

Response - NO
Brief Summary  

Introduction:

Endometriosis is the presence of endometrial glands & stroma outside the uterine cavity. It affects approximately 10% of women of reproductive age with significant impact on physical, mental, and social well-being. The main symptoms include pain, infertility and adnexal mass with the pain symptoms being dysmenorrhea, dyspareunia and chronic pelvic pain. The primary concern of treatment is to reduce the pain symptoms of endometriosis. There are various medical treatment options available including nonspecific non-steroidal anti-inflammatory drugs (NSAIDs), combined oral contraceptives (COC). Recent guidelines recommend the use of either COCs or progestins as a first-line medical treatment for pain associated with endometriosis. There is ample evidence supporting the efficacy in pain control and in reducing the risk of recurrence with both drugs. With the introduction of fourth generation progestins, Dienogest- a synthetic 19-norprogestins with a selective progestin effect the evidences showed extensive improvement in the pain symptoms. It also has anti-estrogenic, anti-gonadotropic, and anti-mineralocorticoid, and antiproliferative effects. Several studies have shown a significant improvement in pain symptoms following treatment with Dienogest. However, regarding the improvement in the pain symptoms there are no comparative study till date about the efficacy in pain relief.

Objectives:

To compare the efficacy in pain relief with Dienogest alone and combination of Dienogest and Ethinyl Estradiol in women with endometriosis.

Methods and materials:

An open-label, randomized, single center, 24-week comparative trial in women between the age of 20-45 years with clinically, radiologically or histologically confirmed endometriosis. Efficacy will be assessed by change in the Visual Analogue Score (VAS) for pain at the end of 12 week and 24 weeks. The other parameters will be assessed are change in the size of endometrioma, self-reported Biberoglu and Behrman (B&B) scale score for pain symptoms of endometriosis, and Improvement in the quality of life by Endometriosis Health Profile-30 (EHP-30) questionnaire. Any additional medications or treatment required for either pain or bleeding will be noted.  

Results:

We will be expecting improvement in the primary and secondary outcome with Dienogest alone or combination of Dienogest and Ethinyl Estradiol. The tolerability and side effects with both drugs will also be assessed.

Conclusion:

Dienogest at 2 mg once a day for 84 days or combination of Dienogest 2mg and Ethinyl Estradiol 30mcg once daily for 84 days will be better in pain symptoms associated with endometriosis.

 
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