Efficacy of Dienogest Versus Oral Contraceptive Pills on Pain Associated With Endometriosis
Primary Purpose
Endometriosis
Status
Unknown status
Phase
Phase 2
Locations
Lebanon
Study Type
Interventional
Intervention
Dienogest 2 MG Oral Tablet
Yasmin
Sponsored by
About this trial
This is an interventional treatment trial for Endometriosis focused on measuring endometriosis, oral contraceptive pills, progestin
Eligibility Criteria
Inclusion Criteria:
- Patients confirmed or suspected of endometriosis on clinical evaluation (VAS score more than 5 and presence of subjective symptoms), surgical or imaging studies, and not taking any pain killer or other hormonal treatment for the moment
- Age 20-45
- Regular menstrual cycles
- The presence of subjective symptoms during menstruation (at least one from among lower abdominal pain, lumbago, defecation pain, nausea, and headache)
- The presence of subjective symptoms during non-menstruation (at least one from among lower abdominal pain, lumbago, defecation pain, dyspareunia, and pain on internal examination).
Exclusion Criteria:
- Undiagnosed genital bleeding
- Use of any hormonal therapy for endometriosis within 16 weeks before enrollment
- A history of severe adverse drug reactions or hypersensitivity to steroid hormone
- Having undergone surgery therapy or surgical examination for endometriosis within a menstrual cycle before the start of medication
- Previous failure of treatment with the OCP used in the current study
- Contraindications to OCP or Dienogest use
- Smokers >35
- A history or complication of thrombosis/embolism
- Migraines with aura
- Depression
- Patients on anti-epileptics
- Diabetes Mellitus with vascular involvement
- Liver diseases
- Known or suspected sex hormone dependent malignancies
- Repeat surgery for endometriosis
- Patient consulting for infertility
- Pregnant or nursing
- Planning for pregnancy in near future.
Sites / Locations
- American University of BeirutRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Dienogest
Oral Contraceptive Pills
Arm Description
Deinogest (Visanne) 2mg/day orally for 24 weeks
Oral contraceptive pill (Yasmin, 0.03mg Ethinyl Estradiol and 3mg Drospirenone) orally daily for 24 weeks
Outcomes
Primary Outcome Measures
Endometriosis-associated pelvic pain
be the absolute change in endometriosis -associated pelvic pain from baseline to end of treatment, assessed by the Visual Analogue Scale (VAS): with "absence of pain" corresponding to the value "0" and "unbearable pain" corresponding to the value "10"
Secondary Outcome Measures
Impact on Quality of life
Outcome quality of life will be assessed using Endometriosis Health Profile 30 (EHP30) with each item of this questionnaire can be answered by choosing one of the following (Never, rarely,sometimes, often and always). The endometriosis health profile is a patient-generated questionnaire in which the items were developed from interviews with women with the condition ( Obtained from Oxford University Press) .
incidence of side effects
Incidence of possible side effects including headache, migraine,nausea, vomiting, abdominal pain/discomfort, breast pain or tenderness, mood swings, premenstrual syndrome, decreased libido, fatigue, weight changes and menstrual irregularities
Patient Tolerability
Assessing tolerability to side effects via numerical scale from zero to ten ( zero not bothersome at all , ten maximum possible)
Full Information
NCT ID
NCT04256200
First Posted
January 15, 2020
Last Updated
April 14, 2021
Sponsor
American University of Beirut Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT04256200
Brief Title
Efficacy of Dienogest Versus Oral Contraceptive Pills on Pain Associated With Endometriosis
Official Title
Efficacy of Dienogest Versus Oral Contraceptive Pills on Pain Associated With Endometriosis
Study Type
Interventional
2. Study Status
Record Verification Date
April 2021
Overall Recruitment Status
Unknown status
Study Start Date
February 7, 2017 (Actual)
Primary Completion Date
November 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
American University of Beirut Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Endometriosis is a chronic inflammatory disease, frequently associated with dysmenorrhea, dyspareunia and abdomino-pelvic pain limiting quality of life. Most medical therapies aim to alleviate the severity of symptoms. Recent guidelines recommend the use of either OCPs or progestins as a first-line treatment of pain associated with endometriosis. The effectiveness of both OCPs and dienogest, a fourth-generation progestin, for endometriosis treatment has been demonstrated. The literature is rich with data comparing the use of Visanne or OCPs to placebo or GnRH analogs. However, there are no head to head studies comparing their efficacy in the management of endometriosis associated pain. The study aims to evaluate if Dienogest (Visanne) is not inferior in efficacy to oral contraceptive pills (Yasmin) in controlling pain associated with endometriosis?
Detailed Description
Endometriosis is defined as the presence of endometrial tissue outside the uterus, which induces a chronic inflammatory reaction. It is an estrogen-dependent associated with pelvic pain and infertility. It is a relatively common chronic gynecological disease that affects approximately 10% of reproductive aged women. Patients with endometriosis often suffer from dysmenorrhea, dyspareunia, dysuria, and chronic abdominal or pelvic pain, resulting in a severely limited quality of life. The aim of most medical therapies is to alleviate the severity of symptoms. Commonly used hormonal therapies include combined oral contraceptives (OCP), progestogens, gonadotropin-releasing hormone (GnRH) agonists, androgens and antiprogestogens, all of which are considered to have similar efficacy but different tolerability profiles, which are often suboptimal. To date, the most widely used agent for the medical treatment of endometriosis is oral contraceptive (albeit off-label). In particular, evidence supporting the efficacy of estrogen-progestin therapy (EP) in pain control and reducing the risk of recurrence in women undergoing surgery for endometriosis. In recent years, the effectiveness of dienogest, a fourth-generation progestin, for endometriosis treatment has been demonstrated. Dienogest seems to be as effective as gonadotrophin-releasing hormone-a (GnRH-a) in terms of endometriosis-related pelvic pain improvement. The aim of this study is to evaluate the efficacy of Visanne versus OCP treatment of endometriosis associated pelvic pain in a double-blinded randomized controlled pilot study. It is a two armed pilot study; each group will include 50 patients. Women with endometriosis will be randomized to receive either DNG (n=50) or OCPs (n=50). The diagnosis of endometriosis will be by clinical evaluation, laparotomy, laparoscopy, or imaging analysis (combination of magnetic resonance imaging and ultrasonography) of endometriotic ovarian chocolate cysts.The first group will receive Deinogest (Visanne) 2mg/day, orally for 24 weeks. The second group will receive monophasic combined OCP (Yasmin, Ethinyl Estradiol and Drospirenone) daily for 24 weeks. The treating physician and the patients will be blinded to the treatment option. The relief of symptoms and efficacy will be evaluated by questionnaire on follow up visits at 3 and 6 month of the treatment. Data collected will be analyzed and compared between the 2 groups. We hypothesize that there will be no difference in pain scores, efficacy and safety between the two treatments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis
Keywords
endometriosis, oral contraceptive pills, progestin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Dienogest
Arm Type
Active Comparator
Arm Description
Deinogest (Visanne) 2mg/day orally for 24 weeks
Arm Title
Oral Contraceptive Pills
Arm Type
Active Comparator
Arm Description
Oral contraceptive pill (Yasmin, 0.03mg Ethinyl Estradiol and 3mg Drospirenone) orally daily for 24 weeks
Intervention Type
Drug
Intervention Name(s)
Dienogest 2 MG Oral Tablet
Other Intervention Name(s)
Visanne
Intervention Description
Deinogest (Visanne) 2mg/day, orally for 24 weeks versus combined OCP (Yasmin, 0.03mg
Intervention Type
Drug
Intervention Name(s)
Yasmin
Other Intervention Name(s)
combined oral contraceptive
Intervention Description
0.03mg Ethinyl Estradiol and 3mg Drospirenone daily for 24 weeks
Primary Outcome Measure Information:
Title
Endometriosis-associated pelvic pain
Description
be the absolute change in endometriosis -associated pelvic pain from baseline to end of treatment, assessed by the Visual Analogue Scale (VAS): with "absence of pain" corresponding to the value "0" and "unbearable pain" corresponding to the value "10"
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Impact on Quality of life
Description
Outcome quality of life will be assessed using Endometriosis Health Profile 30 (EHP30) with each item of this questionnaire can be answered by choosing one of the following (Never, rarely,sometimes, often and always). The endometriosis health profile is a patient-generated questionnaire in which the items were developed from interviews with women with the condition ( Obtained from Oxford University Press) .
Time Frame
6 months
Title
incidence of side effects
Description
Incidence of possible side effects including headache, migraine,nausea, vomiting, abdominal pain/discomfort, breast pain or tenderness, mood swings, premenstrual syndrome, decreased libido, fatigue, weight changes and menstrual irregularities
Time Frame
6 months
Title
Patient Tolerability
Description
Assessing tolerability to side effects via numerical scale from zero to ten ( zero not bothersome at all , ten maximum possible)
Time Frame
6 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients confirmed or suspected of endometriosis on clinical evaluation (VAS score more than 5 and presence of subjective symptoms), surgical or imaging studies, and not taking any pain killer or other hormonal treatment for the moment
Age 20-45
Regular menstrual cycles
The presence of subjective symptoms during menstruation (at least one from among lower abdominal pain, lumbago, defecation pain, nausea, and headache)
The presence of subjective symptoms during non-menstruation (at least one from among lower abdominal pain, lumbago, defecation pain, dyspareunia, and pain on internal examination).
Exclusion Criteria:
Undiagnosed genital bleeding
Use of any hormonal therapy for endometriosis within 16 weeks before enrollment
A history of severe adverse drug reactions or hypersensitivity to steroid hormone
Having undergone surgery therapy or surgical examination for endometriosis within a menstrual cycle before the start of medication
Previous failure of treatment with the OCP used in the current study
Contraindications to OCP or Dienogest use
Smokers >35
A history or complication of thrombosis/embolism
Migraines with aura
Depression
Patients on anti-epileptics
Diabetes Mellitus with vascular involvement
Liver diseases
Known or suspected sex hormone dependent malignancies
Repeat surgery for endometriosis
Patient consulting for infertility
Pregnant or nursing
Planning for pregnancy in near future.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Antoine Abu Musa, M.D.
Phone
+9611350000
Ext
5840
Email
aa06@aub.edu.lb
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Antoine Abu Musa, MD
Organizational Affiliation
American University of Beirut Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
American University of Beirut
City
Beirut
Country
Lebanon
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antoine Abu Musa, MD
Phone
+9611350000
Ext
4840
Email
aa06@aub.edu.lb
12. IPD Sharing Statement
Citations:
PubMed Identifier
34826668
Citation
El Taha L, Abu Musa A, Khalifeh D, Khalil A, Abbasi S, Nassif J. Efficacy of dienogest vs combined oral contraceptive on pain associated with endometriosis: Randomized clinical trial. Eur J Obstet Gynecol Reprod Biol. 2021 Dec;267:205-212. doi: 10.1016/j.ejogrb.2021.10.029. Epub 2021 Oct 30.
Results Reference
derived
Learn more about this trial
Efficacy of Dienogest Versus Oral Contraceptive Pills on Pain Associated With Endometriosis
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