| 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
|
|
|
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
|
|
|
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. |