The Effect of Different Treatment Modalities of Tubal Ectopic Pregnancy on Ovarian Reserve: a Prospective Cohort Study

NCT ID: NCT06471166

Last Updated: 2024-06-24

Study Results

Results pending

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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Recruitment Status

RECRUITING

Total Enrollment

90 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-07-10

Study Completion Date

2025-10-10

Brief Summary

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Detect the effect of different treatment modalities of tubal ectopic pregnancy on ovarian reserve

Detailed Description

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Conditions

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Ectopic Pregnancy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Conservative management

Amh hormone

Intervention Type DIAGNOSTIC_TEST

Ovarian reserve

Medical treatment

Amh hormone

Intervention Type DIAGNOSTIC_TEST

Ovarian reserve

Surgical treatment (Open or laparoscopic salpingectomy)

Amh hormone

Intervention Type DIAGNOSTIC_TEST

Ovarian reserve

Surgical treatment after failed medical treatment (Open or laparoscopic salpingectomy)

Amh hormone

Intervention Type DIAGNOSTIC_TEST

Ovarian reserve

Conservative surgical treatment (salpingotomy, salpingostomy, tubal milking)

Amh hormone

Intervention Type DIAGNOSTIC_TEST

Ovarian reserve

Conservative surgical treatment after failed medical treatment

Amh hormone

Intervention Type DIAGNOSTIC_TEST

Ovarian reserve

Interventions

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Amh hormone

Ovarian reserve

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* The study will include patients aged 18-44 years with known diagnosis or suspicion of diagnosis of tubal ectopic pregnancy (abnormal doubling rates of their b-HCG levels as well as ultrasonographically identified or unidentified gestational sacs outside the uterus)
* Included patients must have capacity to provide informed consent. Given the potential emergent nature of presentation, women will not be recruited if fully informed consent could be compromised due to a highly distressed emotional state or significant hemorrhage necessitating the need for urgent surgery

Exclusion Criteria

1. The use of hormonal contraceptives within two months of enrolment
2. If other surgery was conducted at the time of salpingectomy.
3. If a woman was pregnant at follow up visit for AMH measurement
4. History of previous surgeries of fallopian tubes and/or ovaries
Minimum Eligible Age

18 Years

Maximum Eligible Age

44 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Assiut University

OTHER

Sponsor Role lead

Responsible Party

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Andro Bahgat Heshmat

Resident

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Assiut university

Asyut, , Egypt

Site Status RECRUITING

Countries

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Egypt

Central Contacts

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Andro Bahgat, MD

Role: CONTACT

01283104773

Facility Contacts

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Andro Bahgat, Md

Role: primary

Other Identifiers

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Ectopic pregnancy

Identifier Type: -

Identifier Source: org_study_id

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