Composition for Treating Uterine Fibroid (PP6)

Sponsor
Trieu, Nguyen Thi, M.D. (Other)
Overall Status
Completed
CT.gov ID
NCT04762316
Collaborator
(none)
66
1
2
25
2.6

Study Details

Study Description

Brief Summary

Pregnenolone & Pyridoxal Phosphate (PP6) for treating uterine fibroids in women pregnancy to lost the size fibroids and to dissolve fibroids.

Uterine fibroids are a very common finding in women pregnancy of reproductive age, fibroids fast grow in the first trimester pregnancy. PP6 against the rapid growth of fibroids under the influence of hormones during pregnancy. Use to PP6 think about regulating stable Oestrogen level and to dissolve fibroids.

This is a substantial insight into the pathogenesis of disease, with a clear path toward clinical application, or which would lead to a substantial advance and perfect in management or public health policy.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Uterine fibroids are a very common finding in women's pregnancy of reproductive age fibroids fast grow in the first-trimester pregnancy.

Clinically has shown that:
  • Uterine fibroids are associated with heavy or prolonged menstrual periods, abnormal bleeding between menstrual periods.

  • Fibroids are associated with increased rates of spontaneous miscarriage, premature birth, placenta ablation, malpresentation, labor dysfunction, cesarean section, and postpartum hemorrhage, pain is the most common complication of fibroids uterus during pregnancy.

  • Use the composition that has a sufficient Pregnenolone and combined with Coenzyme Pyridoxal Phosphate, this preparation will soften uterine fibroids and disappear fibroids.

Pregnenolone is produced in the adrenal glands and the central nervous system. Pregnenolone is synthesized from Cholesterol and it is the precursor of Progesterone, Estrogen, and dehydroepiandrosterone (DHEA). In some people Pregnenolone will decrease with age, which will lead to an imbalance between Progesterone, Estrogen, according to research, this imbalance is the cause of abnormal growth of the uterine muscle fibers cells that produce multiple fibroids in the womb. Supplementation Pregnenolone is necessary for women of childbearing and reproductive age, overtime tracking pregnant women but there were fibroids from before pregnancy these fibroids will develop very quickly to stun the fetus many problems in pregnancy, and childbirth, the risk of miscarriage, preterm delivery,...The new drug will maintain a sufficient amount of Pregnenolone natural is the essence from Dioscorea persimilis prain & burkill and associated with a necessary element is Coenzyme Pyridoxal Phosphate. Compound presence in the body will curb the development exceed of the muscle fibers uterus, the muscle fibers in the fibroids will soften, spread out, and disappear fibroids. The uterus returns to its normal state, the fetus will develop naturally.

Research results

  • After 40 weeks of ultrasound examination:

  • 100% of women using PP6 drug have the disappearance of fibroids, only the image of uterine muscle is thicker than usual.

  • 100% of women who received PP6 placebo did not experience any beneficial progress.

  • Through study completion, an average of 40 weeks

Study Design

Study Type:
Interventional
Actual Enrollment :
66 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Selection of women ages 18 to 40, with pregnancy uterine fibroids and pregnancy in the 8th week of pregnancy.Selection of women ages 18 to 40, with pregnancy uterine fibroids and pregnancy in the 8th week of pregnancy.
Masking:
Double (Participant, Investigator)
Masking Description:
The number of post-recruiting people who have fibroids is divided into 2 groups The group of pregnancy uterine fibroids uses drugs under study. The group of pregnancy uterine fibroids uses a placebo
Primary Purpose:
Treatment
Official Title:
Uterine Fibroids Are a Very Common Finding in Women of Reproductive Age. Ready Safety Study Extracts of Plants Pregnenolone & Pyridoxal Phosphate for Treating Uterine Fibroids in Women of Reproductive Age and Women Pregnancy.
Actual Study Start Date :
Jan 1, 2019
Actual Primary Completion Date :
Jan 1, 2021
Actual Study Completion Date :
Feb 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: PP6 Drug

Use PP6 drugs to lose the size of Uterine Fibroids on Women the Pregnancy. Measuring the size of uterine fibroid. Monitor the disappearance of uterine fibroids from 4 - 40 weeks

Drug: PP6
Dosage: -Take 1tablet/2 times/day/in throughout pregnancy.
Other Names:
  • Pregnenolone 40mg & Pyridoxal Phosphate 6mg
  • Placebo Comparator: PP6 Placebo

    Use PP6 placebo to lose the size of Uterine Fibroids on Women the Pregnancy. Measuring the size of uterine fibroid. Monitor the disappearance of uterine fibroids from 4 - 40 weeks

    Device: PP6 Placebo
    Dosage: -Take 1tablet/2 times/day/in throughout pregnancy.
    Other Names:
  • Pregnenolone & Pyridoxal Phosphate Placebo
  • Outcome Measures

    Primary Outcome Measures

    1. Use PP6 drugs to lose the size of Uterine Fibroids on Women the Pregnancy. [40 weeks]

      Measuring the size of uterine fibroid. Monitor the disappearance of benign smooth muscle cell tumors of the uterus

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Procedure to the treatment of fibroids in pregnancy and in women desiring future fertility.
    Exclusion Criteria:
    • Subserosal fibroids may be pedunculated hanging from a stalk inside or outside the uterus.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Saigon Biopharma Company Limited Ho Chi Minh City Vietnam 700000

    Sponsors and Collaborators

    • Trieu, Nguyen Thi, M.D.

    Investigators

    • Principal Investigator: Thi Trieu Nguyen, Dr., Trieu, Nguyen Thi, M.D.

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Trieu, Nguyen Thi, M.D.
    ClinicalTrials.gov Identifier:
    NCT04762316
    Other Study ID Numbers:
    • Removal the Uterine Fibroids
    First Posted:
    Feb 21, 2021
    Last Update Posted:
    May 26, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    Yes
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of May 26, 2022