Recruitment

Recruitment Status
Enrolling by invitation
Estimated Enrollment
Same as current

Summary

Conditions
  • Ovarian Failure
  • Menopause
  • Premature Ovarian Failure 7
  • Menopause Ovarian Failure
  • Menopause, Premature
  • Premature Ovarian Failure 2B
  • Premature Ovarian Failure 5
  • Ovarian Failure Secondary
  • Premature Ovarian Failure 9
  • Premature Ovarian Failure 12
  • Ovarian Failure, Premature
  • Premature Ovarian Failure 6
  • Ovarian Insufficiency
  • Premature Ovarian Failure 11
  • Premature Ovarian Failure 14
  • Premature Ovarian Failure 13
  • Premature Ovarian Failure 2A
  • Ovarian Insufficiency, Primary
  • Premature Ovarian Failure 3
  • Premature Ovarian Failure 8
  • Premature Ovarian Failure
  • Premature Ovarian Failure 1
  • Premature Ovarian Failure 10
  • Premature Ovarian Failure 4
Type
Interventional
Phase
Phase 1Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Pre-post study design: A study group receives the intervention, and the changes in parameters were measured and compared before and after the intervention.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 25 years and 125 years
Gender
Only males

Description

The current study seeks to demonstrate how integrative ovarian rejuvenation program called SEGOVA influence the restoration of hormone stability and increase in the number of follicles in ovarian failure patients. The recruitment of patients and data collection would be performed at three sites: The...

The current study seeks to demonstrate how integrative ovarian rejuvenation program called SEGOVA influence the restoration of hormone stability and increase in the number of follicles in ovarian failure patients. The recruitment of patients and data collection would be performed at three sites: The Special Hospital Jevremova Belgrade, Saint James Hospital Malta, and Remedica Skopje Hospital, Macedonia. A 50-100 of Infertile women with ovarian failure will be included in the period between July 2019 - December 2021. The patients would be coded when entering the program, and all personal information would be protected. Information about medical treatment and background will be held on both paper and electronic case report forms.The result of the procedure will be maintained in the research database with blinding to clinical physician that will perform post procedure follow-up of those patients. In case of a complication, possibly related to treatment, the case will be unblinded. The first day of procedure, autologous platelet rich plasma (PRP) is obtained from 100-120 mL of whole blood. After separation 4 mL of PRP is obtained. Concentration of platelets is optimised on 6-8x baseline and 2-3x leucocytes baseline. For activation of PRP autologous thrombin is used in ratio 1:10. On the same day the laparoscopic cortical resection of the ovary is performed in standard technique. Ovarian cortex sample is minced in a petri dish.The volume of activated PRP (4 mL) is mixed with ovarian fragments and incubated for the next 48h at 37? and 5% CO2. After 48h, the bone marrow sampling from tibia under general anesthesia is performed to obtain bone marrow. After centrifugation the Bone Marrow Aspirate Concentrate (BMAC) with nucleated cells is obtained (3 +/- 1,5 mL). Finally, after the 48h has passed from ovarian cortex tissue incubation, fragmented tissue of the ovary with 4 mL of PRP will be injected together with 3 +/- 1.5 mL BMAC into the subcortical region of the both ovaries as transvaginal ultra sound guided injection. After the procedure, during one year follow up, hormone levels of follicle stimulating hormone (FSH), luteinizing hormone (LH),estradiol (E2), progesterone (PG) and anti-mullerian hormone (AMH) would be measured and the follicle numbers would be monitored to provide insight regarding the ovarian function.To investigate the changes in hormone levels, comparisons of the levels detected prior to the intervention, and 3, 6 and 12 months post-intervention, would be performed using Wilcoxon's rank test. Descriptive statistics will be provided for each variable as mean or median number, frequency, percentage, table or graph. In patients with oocytes retrieved after SEGOVA procedure, standard In Vitro Fertilization protocol would be performed,and fertilization, cleavage and clinical pregnancy rates will be monitored.

Tracking Information

NCT #
NCT04009473
Collaborators
  • Medigroup Health System, Jevremova hospital
  • Saint James Hospital Malta
  • Re-medika Hospital Skoplje
Investigators
Principal Investigator: Aleksandar Ljubic, MD, PhD Medigroup, Belgrade, Serbia