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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02425436
Other study ID # Tibonina/ IUGR
Secondary ID
Status Completed
Phase Phase 2
First received April 21, 2015
Last updated March 20, 2016
Start date May 2014
Est. completion date December 2015

Study information

Verified date March 2016
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority Egypt:Medical School Ethical Review Board
Study type Interventional

Clinical Trial Summary

The use of herbal medicinal products is increasing enormously in recent years, mainly among women, who use them for the most varied purposes, such as in menstrual problems, menopausal symptoms, mood disturbances and to strengthen their bones. Most of these benefits are due to the flavonoids present in these products. These flavonoids have anticarcinogenic, antiviral, antioxidant and antiinflammatory activities, as well as being used in the treatment of osteoporosis, menopausal symptoms and cardiovascular diseases . Besides the benefits from the consumption of flavonoids, little is known about their safety and potentially harmful toxic effects, such as mutagenicity and genotoxicity which might occur if taken in large doses . Safety of Ginkgo biloba during pregnancy or lactation was not criticized in literature. Roasted and raw ginkgo seed were not reported in the evidence-based medicine literature as being either safe or contraindicated in pregnancy or lactation. A higher incidence of postpartum hemorrhage was reported in the literature when associated with a 3-month ingestion of Ginkgo Biloba extract. Flavonoids are components of Ginkgo biloba L. (Ginkgoaceae), a medicinal plant widely used by the population . G. biloba has its origin in China, Korea and Japan where its fruits and leaves have been used as food and medicine for a long time.

The extract of G. biloba (EGb) is composed of different terpene trilactones, i.e., ginkgolides A, B, C, J and bilobalide, many flavonol glycosides, biflavones and alkylphenols . The major flavonoids in the extract are kaempferol, quercetin and isorhamnetin] whose metabolites were found in the blood of rats and in human urine after oral administration of EGb. Due to its actions as an anti-inflammatory and antioxidant, EGb has been largely used in the treatment of Alzheimer's disease, pre-menstrual syndrome, cerebrovascular insufficiency and peripheral arterial occlusive disease . In folk medicine, EGb is used as a vermifuge, to induce labor, for the treatment of bronchitis, chronic rhinitis, chilblains, arthritis and edema . The aim of this study was to evaluate the effect of oral supplementation of Ginkgo Biloba extract on the fetal weight as well as feto-maternal blood flow in cases of intrauterine growth restriction.


Recruitment information / eligibility

Status Completed
Enrollment 226
Est. completion date December 2015
Est. primary completion date October 2015
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 35 Years
Eligibility Inclusion Criteria:

- Pregnant women in their third trimester (28-30 weeks of gestation).

- Pregnant women whose pregnancy was complicated with intra uterine growth restriction (IUGR).

- Normal Doppler indices in uterine, umbilical and middle cerebral arteries at time of recruitment.

Exclusion Criteria:

- Multiple pregnancies,

- Hypertension,

- Fetal congenital anomalies,

- Previous history of congenital anomalies or chromosomal abnormalities.

- Diabetes Mellitus

- Premature pre-labor rupture of membranes

- Antepartum hemorrhage

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Ginkgo Biloba Extract

Other:
Placebo


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Fetal weight (gm) one and half year Yes
Secondary Doppler blood flow changes in uterine arteries indices one and half year Yes
Secondary Doppler blood flow changes in umbilical arteries indices one and half year Yes
Secondary Doppler blood flow changes in middle cerebral artery indices one and half year Yes
See also
  Status Clinical Trial Phase
Terminated NCT02442492 - Sildenafil Therapy In Dismal Prognosis Early-Onset Intrauterine Growth Restriction Phase 2/Phase 3