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Primary Ovarian Insufficiency clinical trials

View clinical trials related to Primary Ovarian Insufficiency.

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NCT ID: NCT04390308 Not yet recruiting - Infertility, Female Clinical Trials

Is There A Role For Mechanical Stimulation In Ovarian Follicular Activation?

Start date: November 23, 2023
Phase:
Study type: Observational

Premature ovarian failure (POI) is a loss of normal function before age 40, leading to infertility and hypoestrogenism. About 1% of women younger than 40 years old and 0.1% before 30 are affected. Most patients already had impaired or complete loss of fecundity when diagnosed. Hence, the treatment of POI is particularly tough. Currently, no optimal regimen exists to ameliorate ovarian function.

NCT ID: NCT04306185 Not yet recruiting - IVF Clinical Trials

Ovarian Fragmentation Study (Crespo Medical Team)

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

This is a study designed to validate Kawamura´s theory and investigation of activation of primordial follicles through ovarian cortex fragmentation. Our aim is to evaluate embryo quality following this procedure in poor ovarian responders and patients with decreased ovarian reserve. Secondary objectives are to assess potential association with the number of oocytes retrieved and pregnancy rates after IVF.

NCT ID: NCT03812913 Not yet recruiting - Pediatrics Clinical Trials

Neuropsychological Assessment of Children and Adolescents With Turner Syndrome

ENEAST
Start date: February 2019
Phase:
Study type: Observational

Turner syndrome (TS) is a rare chromosomal disorder characterized by partial or complete loss of one of the X chromosomes that affects about one in every 2000 female babies born. These young patients described difficulties making friends, understanding others' emotions and intentions, and controlling their own emotions. Difficulties in these domains could led to social withdrawal, to reduced social skills and could have a significant impact on self esteem and mental health as well as on long-term academic and social functioning in affected individuals. The purpose of this project is to identify functional and dysfunctional cognitive and socio-cognitive abilities in these young patients which could account social difficulties described by some of them and their family. To this end, 35 girls with TS and 35 girls with isolated growth hormone deficiency and normal cerebral MRI will be recruited. Subjects will be 7 to 16 years and 11 months of age. Socio-cognitive and cognitive functions will be assessed with neuropsychological and experimental tasks. Questionnaires completed by patient, parents or teacher, will evaluate social and behavioral functioning.

NCT ID: NCT03535480 Not yet recruiting - Clinical trials for Premature Ovarian Failure (POF)

Autologous Bone Marrow Stem Cell Ovarian Transplantation to Restore Ovarian Function in Premature Ovarian Failure

ASCOT-2
Start date: June 2018
Phase: Phase 4
Study type: Interventional

This study aims to recover ovarian function in POF/POI patients. With this pueprose we designed a study protocol including two arms: ASCOT arm, were patients receive the stem cell mobilization treatment with Granulocyte colony stimulating factor (G-CSF) followed by apheresis and ovarian artery catheterism to selectively infuse the stem cells into the ovary and the G-CSF arm including patients that receive the mobilization treatment but not the ovarian artery catheterism to selectively infuse the cells into the ovary.

NCT ID: NCT03412487 Not yet recruiting - Clinical trials for Premature Ovarian Failure

Ovarian Histopathology and Laparoscopic Assessment of Premature Ovarian Failure

Start date: January 2018
Phase: N/A
Study type: Interventional

25 women with Premature Ovarian Failure who attended Fayoum university hospital gynecology outpatient clinic (case group) and another group of 25 women with normal ovarian function (control group). *Pelvic laparoscopy and ovarian biopsy will be done ovarian biopsy preparation For assessment of autoimmune oophoritis, sections were immunostained with anti-LCA (CD45) monoclonal antibody

NCT ID: NCT03207412 Not yet recruiting - Clinical trials for Premature Ovarian Failure

Human Amniotic Epithelial Cells Treatment for Ovarian Insufficiency

Start date: December 22, 2017
Phase: N/A
Study type: Interventional

This project will investigate the safety and effectiveness of human amniotic epithelial cells in primary ovarian insufficiency patients and provide a new cell therapy against infertility.

NCT ID: NCT03034616 Not yet recruiting - Clinical trials for Primary Ovarian Insufficiency

Ovarian Laparoscopic In Vivo Activation of Ovary for Premature Ovarian Insufficiency

OLIVA
Start date: January 2017
Phase: N/A
Study type: Interventional

The OLIVA device will enable to perform shallow slashes on the ovarian cortex in patients undergoing oophorectomy. Prior to the resection of the ovary from the pedicle we will perform 5 parallel slashes 3 cm long. following oophorectomy investigation by the pathologist as to the depth of cuts and proximity to blood vessels and later.

NCT ID: NCT02871986 Not yet recruiting - Clinical trials for Primary Ovarian Insufficiency

Pubertal Induction in Individuals With Hypogonadism

Start date: September 2016
Phase: N/A
Study type: Observational

The investigators wish to explore the variability of uterine, breast and bone outcome markers as surrogates to assess the adequacy of exogenous oestrogen replacement in individuals with hypogonadism.

NCT ID: NCT02757469 Not yet recruiting - Clinical trials for Primary Ovarian Insufficiency

Oral Contraceptives as Infertility Treatments for Premature Ovarian Failure

Start date: May 2016
Phase: N/A
Study type: Interventional

Premature ovarian insufficiency (POI) is a life-changing condition that affects women in their reproductive age. There is a lack of reports which focus on how to improve the reproductive outcome of these women who wish to conceive spontaneously or use assisted conception with their own oocytes. However, one could surmise that it is important to lower gonadotropin levels into the physiological range before embarking on any treatment, even if natural conception is the only choice for the woman/couple.