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Comparison between 20G and 22G for amniocentesis complications

Comparison between 20G and 22G for second trimester amniocentesis in terms of technical aspects and short-term complications

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201510037676N3
Enrollment
400
Registered
2015-10-29
Start date
2015-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Detect of chromosal abnormalities. ??????? ????????? ? ????????

Interventions

Intervention 1: 20 gauge needle will be used for Amniocentesis in group 1. Intervention 2: 22 gauge needle will be used for Amniocentesis in group 2.
Diagnosis
20 gauge needle will be used for Amniocentesis in group 1
22 gauge needle will be used for Amniocentesis in group 2

Sponsors

Vice chancellor for Research
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: single pregnancy;no history of cervical classic failure,hereditary or non-hereditary coagulation disorders, myoma,major fetal anomalies. Exclusion criterion: withdrew from continuing the research

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain intencity. Timepoint: During amniocentesis. Method of measurement: VAS (Visual Analog Scale) system.

Secondary

MeasureTime frame
Abortion under 22 weeks. Timepoint: Up to a week after amniocentesis. Method of measurement: During the phone call.The symptoms of bleeding and pain and miscarriage.;Vaginal bleeding. Timepoint: Up to a week after amniocentesis. Method of measurement: 1-Less than menstrual bleeding 2-menstrual bleedingl.3- more than menstrual bleeding.;Continuous leakage of amniotic fluid. Timepoint: After 6 hours of amniocentesis to 1 week after the procedure. Method of measurement: Observation, ultrasound , nitrazine test.;Chorioamnionitis. Timepoint: Until a week after the procedure. Method of measurement: Uterine tenderness and maternal fever greater than 38°C.;Uterine cramps. Timepoint: After 6 hours of amniocentesis to 1 week after the procedure. Method of measurement: Uterine contractions felt by the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBarband Sharare

Tabriz University of Medical Sciences

salisheri@yahoo.com+98 41351665118

Outcome results

None listed

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