Flexofytol® for the Treatment of Endometriosis- Associated Pain (ENDOFLEX)
Primary Purpose
Endometriosis
Status
Unknown status
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Flexofytol
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Endometriosis focused on measuring Curcuma, Endometriosis-associated pain
Eligibility Criteria
Inclusion Criteria:
- Premenopausal women between the ages of 18 and 51 years
- Ability to comprehend the full nature and purpose of the study
- Signed informed consent
- Diagnosed endometriosis (peritoneal, ovarian or deep-infiltrating endometriosis (DIE))
- By laparoscopy or laparotomy with histological verification diagnosed up to 10 years before screening
- By ultrasound or MRI (ovarian or deep-infiltrating endometriosis, as peritoneal lesions can only be evaluated surgically)
- Moderate to severe pelvic pain (i.e. dysmenorrhea or NMPP of at least 4 on the 1-10 NRS) at least during the past 3 months
- Refusal of hormonal treatments
- The patient must agree to switch from her usual analgesic rescue medication to only the one permitted by the study during screening, treatment and follow-up period
Exclusion Criteria:
- The patient is pregnant or breast feeding or is planning a pregnancy within the treatment period
- Known addiction (alcohol, drugs, pills, etc...)
- Liver or kidney problems
- Known problems of the bile system
- Infection (HIV, Hepatitis, TBC, etc..) or systemic autoimmune diseases
- Known or suspected malignant disease
- Intake of blood-thinning medication (such as heparin or aspirin for example)
- Intake of hormonal contraceptives (oral during the last 4 weeks, injectable: during the last 3 months)
- Patient with a surgical history of hysterectomy, bilateral adnexectomy, endometrial ablation resulting in amenorrhea
Sites / Locations
- General Hospital of Vienna, Medical University of ViennaRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Flexofytol
Placebo
Arm Description
2 capsules containing 42mg of curcumin will be administered twice a day for a duration of 4 months.
2 capsules of the placebo, identical in appearance to Flexofytol, will be administeres twice a day for a duration of 4 months.
Outcomes
Primary Outcome Measures
Change of the average pain score from baseline to 4 months after begin of treatment
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Secondary Outcome Measures
Change in number of days with pain ≥ NRS 4 from baseline to 4 months after begin of treatment
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Alleviation of dyspareunia using the NRS between 0 and 10, from baseline to 4 months after begin of treatment points)
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Alleviation of dysuria using the NRS between 0 and 10 points, from baseline to 4 months after begin of treatment
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Alleviation of dyschezia using the NRS between 0 and 10 points from baseline to 4 months after begin of treatment
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Change in quality of life (using the numerical score of the Endometriosis health profile - EHP 30)
evaluated using a scale of 0 - 100, where 0 indicates the best health status and 100 the worst health status
Change in sexual function (using the numerical score of the female sexual function index - FSFI)
each question answered using a score from 0 to 5, 0 indicating no sexual activity, and, depending on the question, 1 indicating high satisfaction or high frequency, to 5 indicating low satisfaction or low frequency.
Full Information
NCT ID
NCT04150406
First Posted
October 29, 2019
Last Updated
October 31, 2019
Sponsor
Medical University of Vienna
1. Study Identification
Unique Protocol Identification Number
NCT04150406
Brief Title
Flexofytol® for the Treatment of Endometriosis- Associated Pain
Acronym
ENDOFLEX
Official Title
Flexofytol®, a Curcuma Extract, for the Treatment of Endometriosis- Associated Pain: a Randomized, Double Blind, Placebo-controlled Study
Study Type
Interventional
2. Study Status
Record Verification Date
October 2019
Overall Recruitment Status
Unknown status
Study Start Date
October 22, 2019 (Actual)
Primary Completion Date
June 30, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Vienna
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Endometriosis is a benign disease that affects 6-10% of women of reproductive age. The wide range of symptoms observed in patients with endometriosis is due to implantation of endometrial tissue outside the uterine cavity. This ectopic endometrium is subjected to cyclic changes similar to that of eutopic endometrium. Typically, ectopic lesions are found in the pelvis, notably on the ovaries in the form of cysts (endometriomas), as well as the rectouterine and vesicouterine pouch. Lesions have also been described in other parts of the abdomen and in other locations outside the abdominal cavity.
Although endometriosis has also been described in asymptomatic patients, possible symptoms range from mild to severe pain presenting itself as dysmenorrhea, dyspareunia, or dyschezia, or as infertility. Since the clinical picture varies, the treatment of this disease has become quite personalized. Many studies conducted over the past several years have presented different treatment options for the symptoms caused by endometriosis.
Turmeric, which is won from the rootstalks of Curcuma longa, has more than 300 biologically active elements. One of the three main curcuminoids that are derived from turmeric, is curcumin. Several in-vitro and animal studies have described anti-oxidant, anti-inflammatory and anti-angiogenic effects of curcumin.
The main objective for the treatment of endometriosis patients is symptom relief. Treatment options include analgesic therapies, hormonal therapies, laparoscopic surgery or a combination of these. For patients who refuse hormonal therapies however, conservative treatment options are limited.
Curcuma is a substance that has been in use for centuries, especially in ayurvedic and Traditional Chinese Medicine for the treatment of various symptoms, notably for pain alleviation in inflammatory illnesses. Several recently published studies have shown very promising results of Flexofytol for pain alleviation in patients with osteoarthritis, due to its anti-inflammatory and anti-oxidant properties. Due to these properties of curcuma, we aim to analyse if curcuma capsules, sold by the pharmaceutical company Tilman under the name Flexofytol®, can be used to alleviate symptoms in patients suffering from endometriosis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometriosis
Keywords
Curcuma, Endometriosis-associated pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
54 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Flexofytol
Arm Type
Active Comparator
Arm Description
2 capsules containing 42mg of curcumin will be administered twice a day for a duration of 4 months.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
2 capsules of the placebo, identical in appearance to Flexofytol, will be administeres twice a day for a duration of 4 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Flexofytol
Intervention Description
Curcuma extract
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Change of the average pain score from baseline to 4 months after begin of treatment
Description
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Change in number of days with pain ≥ NRS 4 from baseline to 4 months after begin of treatment
Description
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Time Frame
4 months
Title
Alleviation of dyspareunia using the NRS between 0 and 10, from baseline to 4 months after begin of treatment points)
Description
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Time Frame
4 months
Title
Alleviation of dysuria using the NRS between 0 and 10 points, from baseline to 4 months after begin of treatment
Description
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Time Frame
4 months
Title
Alleviation of dyschezia using the NRS between 0 and 10 points from baseline to 4 months after begin of treatment
Description
Pain will be evaluated using the Numeric Rating Scale (NRS), from 0 (no pain) to 10 (worst pain imaginable).
Time Frame
4 months
Title
Change in quality of life (using the numerical score of the Endometriosis health profile - EHP 30)
Description
evaluated using a scale of 0 - 100, where 0 indicates the best health status and 100 the worst health status
Time Frame
4 months
Title
Change in sexual function (using the numerical score of the female sexual function index - FSFI)
Description
each question answered using a score from 0 to 5, 0 indicating no sexual activity, and, depending on the question, 1 indicating high satisfaction or high frequency, to 5 indicating low satisfaction or low frequency.
Time Frame
4 months
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
51 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Premenopausal women between the ages of 18 and 51 years
Ability to comprehend the full nature and purpose of the study
Signed informed consent
Diagnosed endometriosis (peritoneal, ovarian or deep-infiltrating endometriosis (DIE))
By laparoscopy or laparotomy with histological verification diagnosed up to 10 years before screening
By ultrasound or MRI (ovarian or deep-infiltrating endometriosis, as peritoneal lesions can only be evaluated surgically)
Moderate to severe pelvic pain (i.e. dysmenorrhea or NMPP of at least 4 on the 1-10 NRS) at least during the past 3 months
Refusal of hormonal treatments
The patient must agree to switch from her usual analgesic rescue medication to only the one permitted by the study during screening, treatment and follow-up period
Exclusion Criteria:
The patient is pregnant or breast feeding or is planning a pregnancy within the treatment period
Known addiction (alcohol, drugs, pills, etc...)
Liver or kidney problems
Known problems of the bile system
Infection (HIV, Hepatitis, TBC, etc..) or systemic autoimmune diseases
Known or suspected malignant disease
Intake of blood-thinning medication (such as heparin or aspirin for example)
Intake of hormonal contraceptives (oral during the last 4 weeks, injectable: during the last 3 months)
Patient with a surgical history of hysterectomy, bilateral adnexectomy, endometrial ablation resulting in amenorrhea
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Alexandra Perricos, Dr.
Phone
+4369918068650
Email
alexandra.perricos@meduniwien.ac.at
First Name & Middle Initial & Last Name or Official Title & Degree
René Wenzl, Prof. Dr.
Phone
+4314040065190
Email
rene.wenzl@meduniwien.ac.at
Facility Information:
Facility Name
General Hospital of Vienna, Medical University of Vienna
City
Vienna
ZIP/Postal Code
1090
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
René Wenzl, Prof. Dr.
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Flexofytol® for the Treatment of Endometriosis- Associated Pain
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