Clinical Trials Directory

Trials / Completed

CompletedNCT00924885

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
257 (actual)
Sponsor
Vitrolife · Industry
Sex
Female
Age
Healthy volunteers
Not accepted

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.

Detailed description

Although the patient is sedated and local analgesia has been given, transvaginal oocytes retrieval with ultrasound guidance can still cause a lot of pain, both during and after the procedure. To reduce the pain, some clinics prefer to use needles as thin as 0.8 mm (outer diameter, OD). A disadvantage with these needles is the increased aspiration time. Therefore a new needle has been developed that has the possibility to reduce pain without a large increase in aspiration time. The needle has a 50 mm long tip with an outer diameter of 0.9 mm. The remaining part of the needle is 300 mm long with an outer diameter of 1.4 mm.

Conditions

Interventions

TypeNameDescription
DEVICESwemed Follicle Aspiration Set Reduced Single LumenThin tip to penetrate the tissue
DEVICESwemed Follicle Aspiration Set Single Lumen (1.4 mm)Standard (1.4 mm) needle to penetrate the tissue

Timeline

Start date
2009-06-01
Primary completion
2009-12-01
Completion
2009-12-01
First posted
2009-06-19
Last updated
2021-01-26
Results posted
2020-12-10

Locations

4 sites across 1 country: Sweden

Source: ClinicalTrials.gov record NCT00924885. Inclusion in this directory is not an endorsement.

Experience of Pain During Oocyte Retrieval- a Comparison Between Two Aspiration Needles (NCT00924885) · Clinical Trials Directory