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ClinicaI Observation of Induced Abortion With Disposable Tissue Suction Tube

ClinicaI Observation of Induced Abortion With Disposable Tissue Suction Tube

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02847910
Enrollment
500
Registered
2016-07-28
Start date
2016-07-31
Completion date
2017-08-31
Last updated
2021-08-25

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

Conditions

Early Pregnancy

Keywords

tissue suction tube, disposable instrument, induced abortion

Brief summary

The purpose of this study is to explore the clinical effect of disposable tissue suction tube set for induced abortion and make comparison with traditional metal instruments.

Interventions

PROCEDUREthe disposable tissue suction set

Induced abortion is a main backstop for terminating unwanted pregnancies, however, traditional hard metal instruments has lots of insufficiencies such as easily tissue damage, and repeatedly sterilization increases the incidence of cross infection in the hospital what leads to more complications of pelvic inflammation, infertility and so on. Therefore disposable non-metallic instruments are desperately needed as a way to decrease the complications and provide better medical services to patients. So, the investigators want to explore the clinical effect of disposable tissue suction tube set and make comparison with traditional metal instruments.

PROCEDUREtraditional metal instruments of abortion

Induced abortion is a main backstop for terminating unwanted pregnancies. In Chinese hospital, traditional metal instruments are always used during the surgery. So the investigators want to explore the clinical effect of disposable tissue suction tube set and make comparison with traditional metal instruments.

Sponsors

First Affiliated Hospital Xi'an Jiaotong University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 36 Years
Healthy volunteers
No

Inclusion criteria

* premedical abortion diagnosed by ultrasound diagnosed * pregnancy for the first time * 7-9 weeks of pregnancy * voluntary termination of pregnancy * without surgical contraindication

Exclusion criteria

* refuse this clinical trial * with systemic disease such as hypertensive disease, heart disease, diabetes * refuse to terminate the pregnancy

Design outcomes

Primary

MeasureTime frameDescription
blood loss (ml)up to 5-10 minutesIt always takes 5-10 minutes to finish the induced abortion in the outpatient, so the investigators will measure the blood loss during the operation time.
the rate of induced abortion syndrome (%);up to 5-10 minutesIt always takes 5-10 minutes to finish the induced abortion in the outpatient, so the investigators will observe whether induced abortion syndrome happens to our patients during the operation time.

Secondary

MeasureTime frameDescription
evaluate pain grade (0, I, II, III) by questionnaireup to 5-10 minutesThe participants will be asked some questions on questionnaire about feeling to evaluate their pain grade.
rate of leaving bed in 5 min by patient self (%)5 min after the surgery
operation time (minutes)up to 5-10 minutes until the operation finishedmeasure the operation time
the success rate of induced abortion (%)up to 15 days after the surgeryUltrasound and gynecological examinations will be used to calculate the success rate of induced abortion.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026