Experience of Pain During Oocyte Retrieval- a Comparison Between Two Aspiration Needles
- Conditions
- Infertility
- Registration Number
- NCT00924885
- Lead Sponsor
- Vitrolife
- Brief 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.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 257
- The patient has signed an informed consent form before the oocyte retrieval
- The patient is undergoing oocyte retrieval with local anaesthesia
- The patient can speak and understand Swedish
- The patient has previously participated in Vitrolife-needle-01 study
- The patient has a body mass index ≥35
- Other contra indicator for oocyte retrieval
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Visual Analogue Scale After the oocyte retrieval and before the patient leaves the operation room e.g. within a maximum of 30 minutes. Rating of pain was performed by self-assessment by means of Visual Analogue Scale (VAS) consisting of a line oriented vertically on a paper with a range from 0 mm (no pain) to 100 mm (unbearable pain).
- Secondary Outcome Measures
Name Time Method Intervention Because of Bleeding During and directly after oocyte retrieval Vaginal bleeding during or after the procedure was graded subjectively by the physician as (i) less than normal, (ii) normal or (iii) more than normal.
Trial Locations
- Locations (4)
IVF-kliniken Falun
🇸🇪Falun, Sweden
Fertilitetscentrum Göteborg
🇸🇪Göteborg, Sweden
Reproduktionmedicinskt Center, Universitetssjukhuset MAS
🇸🇪Malmö, Sweden
Fertilitetsenheten K59 Karolinska Universitetssjukhuset, Huddinge
🇸🇪Stockholm, Sweden
IVF-kliniken Falun🇸🇪Falun, Sweden