A RCT Study on Autologous Cell Injection Into the Ovaries of Patients With POR

NCT ID: NCT07282288

Last Updated: 2025-12-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 198 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-12-15
• Study Completion Date: 2029-12-01

Brief Summary

Poor ovarian response (POR) is a pathological state where the ovaries do not respond well to the stimulation of gonadotropins. It is mainly characterized by a small number of developing follicles, a high cancellation rate of the ovarian stimulation cycle, a low number of retrieved oocytes, and a low clinical pregnancy rate. Premature ovarian insufficiency (POI) is a special type of this condition and is one of the most difficult infertility diseases to treat. The incidence of POR and POI in reproductive-aged women in China is increasing year by year, making them key and challenging issues in reproductive medicine. New local ovarian cell therapy can improve the microenvironment for follicle development, promote the development and ovulation of "dormant" primordial follicles, and improve the quality of oocytes. This study intends to conduct autologous fat vascular matrix components (SVF) or autologous platelet-rich plasma (PRP) local injection therapy for patients with POR and POI, and conduct a prospective exploratory study to evaluate the safety of this clinical technique. Subsequently, a prospective randomized controlled trial will be conducted to evaluate the safety and efficacy of autologous fat vascular matrix components (SVF) or autologous platelet-rich plasma (PRP) local injection therapy in improving ovarian reserve and IVF-ET outcomes. This study is expected to improve the fertility of patients with POR from the perspective of autologous cell therapy. The autologous SVF and PRP local injection techniques do not involve ethical barriers, are easy to standardize the diagnosis and treatment process and operation system, and are suitable for clinical translation and promotion.

Conditions

Poor Ovarian Response

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

PRP group

Group Type: EXPERIMENTAL

PRP injection

Intervention Type: OTHER

Injecting PRP into the ovaries

SVF group

Group Type: EXPERIMENTAL

SVF injection

Intervention Type: OTHER

Injecting SVF into the ovaries

Control Group

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

PRP injection

Injecting PRP into the ovaries

Intervention Type: OTHER

SVF injection

Injecting SVF into the ovaries

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Women who have fertility requirements and are seeking IVF treatment

2. Age ≤ 45 years old, infertility duration ≥ 1 year

3. Meeting the diagnostic criteria for POI or the Poseidon diagnostic criteria for POR

4. Previous controlled ovarian stimulation resulted in no more than 3 oocytes retrieved and/or no transplantable embryos and/or previous embryo implantation failure ≥ 2 times

5. Uterus and bilateral adnexa are intact

6. BMI 22 - 29 kg/m²

7. Participants must have given informed consent for this study and voluntarily signed a written informed consent form.

Exclusion Criteria

1. Congenital abnormalities of reproductive organs

2. Septicemia, platelet dysfunction syndrome and severe thrombocytopenia and other coagulation disorders or other hematological diseases

3. Suffering from autoimmune diseases or other endocrine disorders, with abnormal thyroid function and uncontrolled condition

4. Having a mass in the adnexal area with an unclear benign or malignant nature

5. Complicated with severe cardiovascular and cerebrovascular diseases, malignant tumors, hematological diseases and mental disorders, patients with impaired function of important organs

6. Those who have used systemic corticosteroids within the last 2 weeks, or used antiplatelet drugs such as aspirin within the last 48 hours

7. In the acute inflammatory stage

8. Those with a history of venous thrombosis or pulmonary embolism during the screening period

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Peking University Third Hospital

OTHER

Sponsor Role: lead

Responsible Party

Ma Caihong

Chief Physician

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

BRWEP2024W094090102

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

IRB00006761-M20250882

Identifier Type: -

Identifier Source: org_study_id