Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
EARLY_PHASE1
35 participants
INTERVENTIONAL
2018-10-10
2018-11-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
DOUBLE
Study Groups
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endometriosis
tissue biopsy from patients (n=10) with endometriosis
No interventions assigned to this group
without endometriosis
tissue biopsy from patients (n=10) without endometriosis
No interventions assigned to this group
Intramuscular progesterone
Intramuscular progestin(20mg)
Progesterone
Different routes of administration of progesterone; Whether there is endometriosis
vaginal progesterone
vaginal progestin (90mg)
Progesterone
Different routes of administration of progesterone; Whether there is endometriosis
oral progesterone
oral progestin(40mg)
Progesterone
Different routes of administration of progesterone; Whether there is endometriosis
Interventions
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Progesterone
Different routes of administration of progesterone; Whether there is endometriosis
Eligibility Criteria
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Inclusion Criteria
control group: Laparoscopic bilateral salpingectomy was performed due to ectopic pregnancy, benign ovarian changes and other reasons, with the exception of endometriosis during the operation.Regular menstruation, no rule vaginal bleeding;Ovarian reserve function is normal
2. progesterone group Women with hypothalamic amenorrhea or premature ovarian failure;Ages 18-40
Exclusion Criteria
18 Years
40 Years
FEMALE
Yes
Sponsors
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Peking Union Medical College Hospital
OTHER
Responsible Party
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Locations
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Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, China
Countries
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Facility Contacts
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Other Identifiers
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yuqi03029
Identifier Type: -
Identifier Source: org_study_id
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