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Prediction of Preeclampsia & Other Obstetric Complications by Serum Homocysteine & Doppler

K

Kasr El Aini Hospital

Status

Unknown

Conditions

Preeclampsia
IUGR

Study type

Observational

Funder types

Other

Identifiers

NCT02541110
Obgyn. .

Details and patient eligibility

About

Second trimester homocysteine & uterine artery doppler will be assessed& the cases will be followed up till delivery for development of preeclampsia, IUGR(intra-uterine growth retardation) & other obstetric complications.

Full description

Spontaneous pregnancies with no risk factors will be included. Fasting plasma total homocysteine level samples will be collected between 15th & 19th weeks.

Uterine artery doppler between 18th & 22nd weeks.

Method 1: Screen positive cases will be considered if homocysteine level above 6.3umol/l

Method 2: Screen positive cases will be considered if they had bilateral notches and a mean resistivity index (RI) above 0.55, or unilateral notches and a mean RI above 0.65, or absence of notches and a mean RI above 0.7.

Method 3: Screen positive cases will be considered if they had bilateral notches and a mean RI above 0.55, or unilateral notches and a mean RI above 0.65, or absence of notches and a mean RI above 0.7 combined with homocysteine cut off value of 6.3umol / l.

Enrollment

200 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • spontaneous pregnancies with no risk factors

Exclusion criteria

  • multiple pregnancies
  • non intact renal function
  • hypertension
  • diabetes
  • folic acid supplements
  • antifolate drugs

Trial contacts and locations

0

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Central trial contact

suzy abdelaziz, M.D.

Data sourced from clinicaltrials.gov

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