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The primary investigator moved from academic practice to join a private group, and could not get any one to take over as PI for the study.
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Progestin-induced endometrial shedding (PIES) followed by clomiphene citrate is fertility treatment of choice in anovulatory women with polycystic ovary syndrome (PCOS). However, some preliminary data suggest that skipping PIES could result in a higher live birth rate. The investigators are performing the first randomized controlled trial to find out if skipping the use of progestin during fertility treatment of anovulatory PCOS women is associated with improved pregnancy and live birth rates compared to the traditional approach of using progestin prior to use of clomiphene citrate.
This is a prospective randomized trial of clomiphene citrate (CC) preceded by progestin-induced endometrial shedding (PIES) vs CC without PIES in the treatment of infertility in patients with PCOS, for up to 5 treatment cycles.
Participants will be randomized to receive either progestin followed by CC starting on day 3 of the induced menses, or CC without induced menses. Study participants will be monitored at regular 2 to 4 wks intervals for response to medication using ultrasound and hormonal parameters. The maximum dose of CC will not exceed 750 mg/cycle. Treatment will not exceed 5 ovulatory cycles. Participants who are resistant to 150 mg of CC will exit the study.
170 anovulatory PCOS women actively seeking pregnancy, aged 18 through 40 years will be enrolled and randomized in a 1:1 treatment ratio into the two study arms. Anovulation will be the only infertility factor in all patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group A (No PIES) | Experimental | Subjects randomized to this group will receive clomiphene citrate (CC) without using progestin throughout their treatment course.
|
|
| Group B (PIES Group) | Active Comparator | Women randomized to this group will receive progestin to induce endometrial shedding before starting any doses of clomiphene citrate (CC)
|
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Progestin | Drug |
|
| |
| Measure | Description | Time Frame |
|---|---|---|
| Live Birth | Delivery of a viable infant after 24 weeks of pregnancy | Within 36 weeks of a positive pregnancy test |
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Inclusion
Exclusion
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| Name | Affiliation | Role |
|---|---|---|
| Albert Asante, MD, MPH | University of Illinois at Chicago | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Illinois at Chicago | Chicago | Illinois | 60612 | United States |
The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available.
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| ID | Title | Description |
|---|---|---|
| FG000 | Group A (No PIES) | Subjects randomized to this group will receive clomiphene citrate (CC) without using progestin throughout their treatment course.
Clomiphene Citrate |
| FG001 | Group B (PIES Group) | Women randomized to this group will receive progestin to induce endometrial shedding before starting any doses of clomiphene citrate (CC)
Progestin Clomiphene Citrate |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available.
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| ID | Title | Description |
|---|---|---|
| BG000 | Group A (No PIES) | Subjects randomized to this group will receive clomiphene citrate (CC) without using progestin throughout their treatment course.
Clomiphene Citrate |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available. |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Live Birth | Delivery of a viable infant after 24 weeks of pregnancy | The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available. | Posted | Within 36 weeks of a positive pregnancy test |
|
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The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available.
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Group A (No PIES) | Subjects randomized to this group will receive clomiphene citrate (CC) without using progestin throughout their treatment course.
Clomiphene Citrate |
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The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Albert Asante, MD MPH | UIC | 3123552634 | akdasante@yahoo.com |
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| ID | Term |
|---|---|
| D011085 | Polycystic Ovary Syndrome |
| D007246 | Infertility |
| D000858 | Anovulation |
| ID | Term |
|---|---|
| D010048 | Ovarian Cysts |
| D003560 | Cysts |
| D009369 | Neoplasms |
| D010049 | Ovarian Diseases |
| D000291 |
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| ID | Term |
|---|---|
| D011372 | Progestins |
| D017258 | Medroxyprogesterone Acetate |
| D002996 | Clomiphene |
| ID | Term |
|---|---|
| D006728 | Hormones |
| D006730 | Hormones, Hormone Substitutes, and Hormone Antagonists |
| D045505 | Physiological Effects of Drugs |
| D020228 | Pharmacologic Actions |
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| Clomiphene Citrate |
| Drug |
|
|
| BG001 | Group B (PIES Group) | Women randomized to this group will receive progestin to induce endometrial shedding before starting any doses of clomiphene citrate (CC)
Progestin Clomiphene Citrate |
| BG002 | Total | Total of all reporting groups |
| years |
| Sex: Female, Male | The study was terminated and data cannot be retrieved as the software where data has been stored has been upgraded. We have exhausted efforts to retrieve the data from this software and no study data are available |
|
| Group B (PIES Group) |
Women randomized to this group will receive progestin to induce endometrial shedding before starting any doses of clomiphene citrate (CC)
Progestin Clomiphene Citrate |
|
| 0 |
| 0 |
| 0 |
| 0 |
| 0 |
| 0 |
| EG001 | Group B (PIES Group) | Women randomized to this group will receive progestin to induce endometrial shedding before starting any doses of clomiphene citrate (CC)
Progestin Clomiphene Citrate | 0 | 0 | 0 | 0 | 0 | 0 |
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| Adnexal Diseases |
| D005831 | Genital Diseases, Female |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D000091662 | Genital Diseases |
| D006058 | Gonadal Disorders |
| D004700 | Endocrine System Diseases |
| D020164 | Chemical Actions and Uses |
| D008525 | Medroxyprogesterone |
| D006908 | Hydroxyprogesterones |
| D011374 | Progesterone |
| D011282 | Pregnenediones |
| D011283 | Pregnenes |
| D011278 | Pregnanes |
| D013256 | Steroids |
| D000072473 | Fused-Ring Compounds |
| D011083 | Polycyclic Compounds |
| D013267 | Stilbenes |
| D001597 | Benzylidene Compounds |
| D001555 | Benzene Derivatives |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |