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Status unknownNCT04684680Updated Aug 9, 2021

The Role of Zamzam Water in Idiopathic Oligohydramnios

An interventional study of zamzam water and tap water in Oligohydramnios, sponsored by Aswan University Hospital. Status unknown at 1 site in Egypt. Open to female participants aged 18 Years to 40 Years. Per ClinicalTrials.gov, last updated 2021-08-09.

Sponsored by Aswan University Hospital · Not applicable, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Aug 2021), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
120
Allocation
Randomized
Ages
18 Years to 40 Years
Sex
Female
01

Study summary

The aim of this study is to evaluate the efficacy of drinking zamzam water versus tap water in increasing the AF index in women with oligohydramnios.

Read the detailed description

Oligohydramnios refers to decrease in amniotic fluid and it is defined as a deepest fluid pocket of less than 2 cm or an amniotic fluid index of 5 cm or less. Oligohydramnios complicates 0.5% to 8% of pregnancies, and 12 % if postdates When it occurs in first half of pregnancy it is associated with birth defects while in second half it causes poor fetal growth, malpresentations , FHR decelerations , MAS , Fetal suicidal syndrome and increases cesarean section and management and prognosis depend on gestational age

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Conditions studied

  • Oligohydramnios

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03

In context

Oligohydramnios

25 studies on the registry are indexed under Oligohydramnios; 5 are open to participants now.

This study's planned enrollment of 120 is above the median of 91 across 16 interventional studies indexed under Oligohydramnios.

Browse Oligohydramnios studies →

Lead sponsor

Aswan University Hospital is the lead sponsor of 97 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 40 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • pregnant female with idiopathic oligohydramnios

Exclusion criteria

Exclusion Criteria:

  • patients with medical disorder
  • congenital anomalies
  • premature rupture of membrane
  • Patient refuse to participate
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Experimental
    zamzam water

    patient will receive the normal need of daily requirement of water (2.5 liter) in form of zamzam water till patients deliver or till term

    Dietary Supplement: zamzam water

  • Active comparator
    tap water

    will receive the normal need of daily requirement of water (2.5 liter) in form of tap water

    Dietary Supplement: tap water

Interventions

  • Dietary supplementzamzam water

    will receive the normal need of daily requirement of water (2.5 liter) in form of zamzam water till patients deliver or till term

    Also known as: study group

  • Dietary supplementtap water

    will receive the normal need of daily requirement of water (2.5 liter) in form of tap water

    Also known as: Active Comparator

06

What researchers measure

Primary outcomes

  1. amniotic fluid index

    the change of the amniotic fluid volume

    Time frame: 10 weeks

07

Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jan 2021 (actual). Primary completion is estimated for Sep 2021, 8 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 5, 2020
First posted
Dec 24, 2020
StartActual
Jan 1, 2021
Primary completionEst.
Sep 30, 2021
CompletionEst.
Nov 1, 2021
Last update
Aug 9, 2021
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 9, 2021, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04684680
Lead sponsor
Aswan University Hospital
Responsible party
hany farouk (A Professor, Aswan University Hospital) — Principal investigator
First posted
Dec 24, 2020
Start date
Jan 1, 2021
Primary completion
Sep 30, 2021 (estimated)
Completion
Nov 1, 2021 (estimated)
Last update
Aug 9, 2021

Study contacts

Hany f Sallam, md
Contact
hanygyne@yahoo.com
+201022336052 ext. 002
nahla w shady, md
Contact
nahlagyn@yahoo.com
+201022336052 ext. 002
nahla w shady, md
study chair · Aswan universirty

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Aug 2021. You cannot join it, but the record below documents what was studied.

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