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Experience of Pain During Oocyte Retrieval- a Comparison Between Two Aspiration Needles

NCT00924885 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 257

Last updated 2021-01-26

Study results available
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Summary

The purpose of the study is to compare the pain experience between the patients that have had their transvaginal oocytes retrieval with ultrasound guidance performed with reduced single lumen needle (Vitrolife Sweden AB, Gothenburg) with the patients that have had follicle aspiration needle, 1.4 outer diameter (Vitrolife Sweden AB, Gothenburg), during the procedure.

Conditions

Interventions

DEVICE

Swemed Follicle Aspiration Set Reduced Single Lumen

Thin tip to penetrate the tissue

DEVICE

Swemed Follicle Aspiration Set Single Lumen (1.4 mm)

Standard (1.4 mm) needle to penetrate the tissue

Sponsors & Collaborators

  • Vitrolife

    lead INDUSTRY

Principal Investigators

  • Torbjörn Hillensjö, MD PhD · Fertility Center Scandinavia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-06-30
Primary Completion
2009-12-31
Completion
2009-12-31

Countries

  • Sweden

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00924885 on ClinicalTrials.gov