Autologous Platelet-rich Plasma for Clomiphene Citrate-induced Thin Endometrium
Primary Purpose
Infertility, Female, Associated With Anovulation
Status
Completed
Phase
Phase 2
Locations
Egypt
Study Type
Interventional
Intervention
clomiphene citrate
Saline cervical flushing
Intrauterine Autologous platelet-rich plasma
Sponsored by
About this trial
This is an interventional treatment trial for Infertility, Female, Associated With Anovulation
Eligibility Criteria
Inclusion Criteria:
- Women with clomiphene citrate failure (defined as at least previous 3 ovulatory cycles with clomiphene citrate, with no pregnancy),
- persistently thin endometrium (less than 7 millimeters in at least 3 cycles).
- normal baseline Follicle Stimulating Hormone, Luteinizing Hormone, and free testosterone levels, patent tubes by hysterosalpingography, and satisfactory male semen analysis
Exclusion Criteria:
- previous ovarian surgery;
- endocrine disorders ;
- pelvic pathologies;
- chronic hepatic, cardiovascular, or renal disease;
- other factors of infertility and
- use of gonadotropins or hormonal contraception through the latest 6 months.
Sites / Locations
- Banha Faculty Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Clomiphene citrate only
Platelet-rich plasma plus Clomiphene
Arm Description
Infertile women (30 women) with prior clomiphene citrate failure (ovulation was documented without conception), with thin endometrium (<7mm) in at least 3 cycles. Saline cervical flushing will be done at cycle day 8 and 10 to convince patient-blinded procedure.
Women who did not conceive on the Clomiphene citrate-only cycle will receive Clomiphene citrate 100 mg/ day starting from the third day of the cycle. Intrauterine Autologous platelet-rich plasma will be done on the cycle days 8 and 10.
Outcomes
Primary Outcome Measures
Endometrial thickness
Transvaginal sonographic estimation of maximal distance traversing endometrial- myometrial interphase on each endometrial stripe in a -midsagittal plane in the uterine fundus.
Secondary Outcome Measures
Power Doppler estimation of endometrial and sub-endometrial vascularity
Endometrial and sub-endometrial vascularity signals will be evaluated using the power Doppler.
Clinical pregnancy rate
Recognizing pregnancy through positive urinary HCG test plus sonographic detection of cardiac pulsations
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03770026
Brief Title
Autologous Platelet-rich Plasma for Clomiphene Citrate-induced Thin Endometrium
Official Title
Intrauterine Infusion of Autologous Platelet-rich Plasma to Prevent a Thin Endometrium in Infertile Women Undergoing Clomiphene Citrate Therapy: a Pilot Prospective Self-controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
January 1, 2019 (Actual)
Study Completion Date
January 1, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Benha University
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
This is a prospective self-controlled clinical study. Women with clomiphene Citrate failure with thin endometrium less than 7 millimeters for at least 3 cycles will be selected (N = 30). Patients will receive 2 ovarian stimulation cycles with Clomiphene citrate (CC) 100 mg/ day for 5 days from cycle day 3. A control cycle (CC only cycle) woman will continue on CC alone plus cervical irrigation of cervix with 1 ml of 0.9% normal saline at cycle day 8 and 10 to assure patient-blinded method. The study group, the same will be done plus the intrauterine infusion of Autologous platelet-rich plasma (PRP) in 8th and 10th days of the cycle. In both groups, the endometrial thickness and Power Doppler evaluation of their endometrial and sub-endometrial blood flow will be measured on the day of Human Chorionic Gonadotropin (HCG) administration.
Detailed Description
This is a pilot prospective self-controlled clinical trial. Women with Clomiphene Citrate failure with documented thin endometrium less than 7 millimeters for at least 3 stimulation cycles will be chosen (N = 30). Patients will experience 2 ovarian stimulation cycles with Clomiphene citrate (CC) in a dose of 100 mg/ day for 5 days starting from cycle day 3. A control cycle (CC only cycle) woman will continue on Clomiphene Citrate alone plus cervical irrigation of cervix with 1 ml of 0.9% normal saline at cycle day 8 and 10 to confirm patient-blinded process.
The study group, the same will be done in addition to the intrauterine infusion of with Autologous platelet-rich plasma (PRP) in 8th and 10th days of the cycle.
In both groups, the endometrial thickness and Power Doppler evaluation of their endometrial and sub-endometrial blood flow will be measured on the day of HCG administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Female, Associated With Anovulation
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Masking
Participant
Allocation
Non-Randomized
Enrollment
30 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Clomiphene citrate only
Arm Type
Active Comparator
Arm Description
Infertile women (30 women) with prior clomiphene citrate failure (ovulation was documented without conception), with thin endometrium (<7mm) in at least 3 cycles. Saline cervical flushing will be done at cycle day 8 and 10 to convince patient-blinded procedure.
Arm Title
Platelet-rich plasma plus Clomiphene
Arm Type
Experimental
Arm Description
Women who did not conceive on the Clomiphene citrate-only cycle will receive Clomiphene citrate 100 mg/ day starting from the third day of the cycle. Intrauterine Autologous platelet-rich plasma will be done on the cycle days 8 and 10.
Intervention Type
Drug
Intervention Name(s)
clomiphene citrate
Other Intervention Name(s)
Clomiphene
Intervention Description
Clomiphene citrate-only arm: Patients will receive Clomiphene citrate induction (in a dose of 100 mg/day starting from day 3 of the cycle for 5 days). Sonographic assessment of endometrial thickness together with Power Doppler evaluation endometrial and sub-endometrial blood flow a will be done in the Day of HCG injection.
Intervention Type
Drug
Intervention Name(s)
Saline cervical flushing
Other Intervention Name(s)
Saline
Intervention Description
Cervical irrigation with 1 ml of 0.9% normal saline will be done at cycle day 8 and 10 to convince patient-blinded procedure.
Intervention Type
Biological
Intervention Name(s)
Intrauterine Autologous platelet-rich plasma
Other Intervention Name(s)
Platelet-rich plasma
Intervention Description
Under complete aseptic cares and ultrasound supervision, Autologous platelet-rich plasma (0.5 - 1 ml) was immediately injected into the uterine cavity using an intrauterine insemination catheter in the cycle days 8 and 10. The Autologous platelet-rich plasma is prepared in collaboration with the Department of Clinical Pathology, Faculty of Medicine, Benha University.
Primary Outcome Measure Information:
Title
Endometrial thickness
Description
Transvaginal sonographic estimation of maximal distance traversing endometrial- myometrial interphase on each endometrial stripe in a -midsagittal plane in the uterine fundus.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Power Doppler estimation of endometrial and sub-endometrial vascularity
Description
Endometrial and sub-endometrial vascularity signals will be evaluated using the power Doppler.
Time Frame
1 day
Title
Clinical pregnancy rate
Description
Recognizing pregnancy through positive urinary HCG test plus sonographic detection of cardiac pulsations
Time Frame
At the end of a 28-day menstrual cycle.
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Women with clomiphene citrate failure (defined as at least previous 3 ovulatory cycles with clomiphene citrate, with no pregnancy),
persistently thin endometrium (less than 7 millimeters in at least 3 cycles).
normal baseline Follicle Stimulating Hormone, Luteinizing Hormone, and free testosterone levels, patent tubes by hysterosalpingography, and satisfactory male semen analysis
Exclusion Criteria:
previous ovarian surgery;
endocrine disorders ;
pelvic pathologies;
chronic hepatic, cardiovascular, or renal disease;
other factors of infertility and
use of gonadotropins or hormonal contraception through the latest 6 months.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmed Walid A Morad
Organizational Affiliation
Banha Faculty of Medicine, Banha Univerisity
Official's Role
Principal Investigator
Facility Information:
Facility Name
Banha Faculty Hospital
City
Banha
State/Province
Alkalubia
ZIP/Postal Code
13511
Country
Egypt
12. IPD Sharing Statement
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Autologous Platelet-rich Plasma for Clomiphene Citrate-induced Thin Endometrium
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