Uterus Transplantation From Deceased Donor - Gothenburg III

NCT ID: NCT03581019

Last Updated: 2024-06-21

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

1 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-06-17

Study Completion Date

2023-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Deceased donor uterus transplantation will be offered to patients that have either been excluded from Gothenburg II because of donor criteria or because of early graft failure in Gothenburg I and II

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Absolute Uterine Factor Infertility Transplantation Mrk Anomaly

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Observational study
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Uterus transplantation

Uterus transplantation

Group Type EXPERIMENTAL

uterus transplantation

Intervention Type PROCEDURE

uterus transplantation from deceased donor

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

uterus transplantation

uterus transplantation from deceased donor

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* initially included with IVF and excluded by donor issues of Gothenburg I or II
* initially included and excluded by early graft failure of Gothenburg I or II
* age \< 40 years
* no systemic disease
* no standing medication
* satisfactory ovarian reserve
* BMI \<35 and at BMI 30-35 waist circumference of \< 82 cm
* absolute uterine factor infertility
* psychological stable


* brain death and suitable as multiorgan donor
* acceptance for donation of uterus from family or previously by patient
* age \<55 years
* at least one normal pregnancy and childbirth
* no previos malignancy
* no systemic disease
* no previous major surgery inn abdomen or on uterus
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Sahlgrenska University Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mats Brännström

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Mats Brännström

Role: PRINCIPAL_INVESTIGATOR

Göteborg University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Sahlgrenska University Hospital

Gothenburg, , Sweden

Site Status

Mats Brännström

Gothenburg, , Sweden

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Sweden

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Sahlgrenska-DD-UTx

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.