Investigation of hypo gastric arterial ligation in placenta accreta disorders

Investigation the outcomes of hypogastric arterial ligation before hysterectomy in patients with placenta accreta compare to healthy control

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190123042467N1

Enrollment

Registered

2019-06-14

Start date

2018-12-22

Completion date

Unknown

Last updated

2019-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Placenta adherent disorder. Third-stage hemorrhage

Interventions

Intervention 1: Intervention group is consist of pregnant women with placenta accreta disorder who are candidate for hypo-gastric arterial ligation before hysterectomy. Intervention 2: Control group:

Eligibility

Sex/Gender

Female

Age

15 Years to 49 Years

Inclusion criteria

Inclusion criteria: ?Diagnosis of placenta accreta disease by two experienced gynecologists by Color Doppler Ultrasonography Awareness of the patient and her/his family from the study and signing the consent form

Exclusion criteria

Exclusion criteria: Patient's dissatisfaction for participating in the study

Design outcomes

Primary

Measure	Time frame
Amount of blood loss during operation. Timepoint: Immediately after intervention. Method of measurement: The amount of blood inside the aspirator.;Frequency of deep vein thrombosis. Timepoint: Seven days after operation. Method of measurement: Duplex ultrasonography.;Amount of used blood products during operation. Timepoint: End of operation. Method of measurement: Direct counting.;Operation time. Timepoint: End of operation. Method of measurement: Timer.;Time of hospitalization. Timepoint: Seven days after operation. Method of measurement: Investigation of medical record.	—

Measure

Time frame

Amount of blood loss during operation. Timepoint: Immediately after intervention. Method of measurement: The amount of blood inside the aspirator.;Frequency of deep vein thrombosis. Timepoint: Seven days after operation. Method of measurement: Duplex ultrasonography.;Amount of used blood products during operation. Timepoint: End of operation. Method of measurement: Direct counting.;Operation time. Timepoint: End of operation. Method of measurement: Timer.;Time of hospitalization. Timepoint: Seven days after operation. Method of measurement: Investigation of medical record.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Niakan

Esfahan University of Medical Sciences

niakanzahra@gmail.com+98 31 3668 0048

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026