Intralipid Related Effect on NKcells in Patients With Unexplained Recurrent Spontaneous Abortion


Evaluating the effect of intralipid on the natural killer cells

Full Title of Study: “Intralipid Related Effect on NKcells in Patients With Unexplained Recurrent Spontaneous Abortions”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: January 20, 2018

Detailed Description

This study will done on women with recurrent spontaneous abortions having increased NKCELLS activity and evaluate the effect of Intralipid on them after re-estimation of NKcells activity again after one week of Intralipid adminstration


  • Drug: Intralipid
    • Adose of intralipid given and rechecking NKcells activity

Arms, Groups and Cohorts

  • Experimental: One armed
    • One group of patient will take Intralipid for all

Clinical Trial Outcome Measures

Primary Measures

  • Change in NK cells activity after injection of intralipid
    • Time Frame: One week
    • NK cells is measured before and after injection of intralipid and is noticed for change in activity

Participating in This Clinical Trial

Inclusion Criteria

  • All women icluded having recurrent spontaneous abortions equal or more than twice.
  • Alittle women having increased NKCELLS activity.

Exclusion Criteria

  • Any other diseases causing miscarriage as autoimmune (lupus erythematosus or antiphospholipid antibodies syndrome )or endocrinopathy (diabetes mellitus, thyroid disorders and hyperprolactinaemia)or thrombophilia (factor v leiden mutation, protein c or s deficiency, prothrombin G20210A mutation, antithrombin III deficiency ) or abnormal karyotyping to one or both of parents or previous history of hormonal contraception or intrauterine device usage at last 3 months or any contraindications for intralipid usage.

Gender Eligibility: Female

Women with recurrent spontaneous abortions

Minimum Age: 18 Years

Maximum Age: 38 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Ahmed Mohamed Bahaa Eldin Ahmed
  • Collaborator
    • Ain Shams Maternity Hospital
  • Provider of Information About this Clinical Study
    • Sponsor-Investigator: Ahmed Mohamed Bahaa Eldin Ahmed, Clinical professor – Ain Shams Maternity Hospital
  • Overall Official(s)
    • Hassan T Khairy, Professor, Study Director, Hassan Tawfik office
  • Overall Contact(s)
    • Sobhy R Mohammed, MBBCH, 01003815460,

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