PRP in Intracytoplasmic Sperm Injection

NCT ID: NCT04354363

Last Updated: 2020-04-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-04-22

Study Completion Date

2021-03-01

Brief Summary

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Infertility is a major problem nowadays

Detailed Description

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ovarian and uterine factor of infertility are very hard to treat

Conditions

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Infertility

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

A randomized controlled trial
Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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PRP

women who will receive PRP before ICSI

Group Type ACTIVE_COMPARATOR

Platelet rich plasma

Intervention Type OTHER

Giving women PRP before ICSI

No PRP

women who willnot receive PRP before ICSI

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Platelet rich plasma

Giving women PRP before ICSI

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* women with primary infertility

Exclusion Criteria

* women with unexplained infertility
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Aljazeera Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Mahmoud Alalfy, PhD

Role: STUDY_CHAIR

Algezeera hospitaland National Research Centre ,Egypt

Locations

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Algazeerah

Giza, , Egypt

Site Status

Countries

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Egypt

Central Contacts

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Mahmoud Alalfy, PhD

Role: CONTACT

01002611058

Facility Contacts

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Mahmoud Alalfy, master

Role: primary

+201002611058

Ahmed Elgazzar, M.D

Role: backup

+201014005959

Other Identifiers

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ICSI in poor reserve

Identifier Type: -

Identifier Source: org_study_id

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