Influence Instillation Plasma Rich in Growth Factors in Endometrial Cavity Endometrial Development in Assisted Reproduction.

NCT ID: NCT02996760

Last Updated: 2022-04-07

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

TERMINATED

Clinical Phase

PHASE3

Total Enrollment

22 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-14

Study Completion Date

2021-12-31

Brief Summary

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Women in assisted reproduction treatment they receive own or donated embryos and presenting an endometrial development less than 5 mm despite having received treatment with estrogen therapy knowing the clinical value of using the PRGF-Endoret therapy and endometrial level applications to improve endometrial thickness endometrial preparations for embryo transfer.

Detailed Description

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Conditions

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Endometrial Development

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Endometrium with less than 5mm

Women receiving cycle of oocytes outside or embryos (own / others), in the treatment of substituted cycle type.

Less than 5mm despite 10 days with standard doses of estrogen

Group Type EXPERIMENTAL

Growth Factor, Platelet-Derived

Intervention Type DRUG

0,5 mL, vaginal use , 3 dose number

Endometrium with more than 5mm

Women receiving cycle of oocytes outside or embryos (own / others), in the treatment of substituted cycle type.

More than 5mm despite 10 days with standard doses of estrogen

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Growth Factor, Platelet-Derived

0,5 mL, vaginal use , 3 dose number

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Women receiving cycle of oocytes outside or embryos (own / others), in the treatment of substituted cycle type.
* Less than 5mm despite 10 days with standard doses of estrogen therapy (6mg / 24h) Endometrio

Exclusion Criteria

* History of pelvic inflammatory disease
* Risk of infection
Minimum Eligible Age

18 Years

Maximum Eligible Age

49 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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IVI Bilbao

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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IVI Bilbao

Leioa, Vizcaya, Spain

Site Status

Countries

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Spain

Other Identifiers

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1404-BIO-019-MF

Identifier Type: -

Identifier Source: org_study_id

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