Pain Assessment of the IVF Needle
Recruiting
- Conditions
- involuntary childlessnessSubfertility10029903
- Registration Number
- NL-OMON47399
- Lead Sponsor
- Jeroen Bosch Ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 93
Inclusion Criteria
- Indication for IVF/ICSI
- Female age between 18 and 42 years
- Informed consent
- Normal position of the ovaries
Exclusion Criteria
- A previous IVF or ICSI treatment
- Endometriosis
- BMI > 35
- Use of painmedication
- OHSS
- Operation in lower abdomen
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>Primarily there will be a look at the difference in pain scores with the use of<br /><br>a thinner needle. </p><br>
- Secondary Outcome Measures
Name Time Method <p>Secondary outcomes were differences in: oocyte quality, total procedure time,<br /><br>follow procedure/fertilization, demand for additional analgesia during the<br /><br>procedure, time to resign after puncture, pain medication days after puncture,<br /><br>possible influence of age and/or weight on pain score, relationship between<br /><br>pain score and indication puncture, impact doctor performing puncture on pain<br /><br>score and whether the *overall* savings for the economy, considering<br /><br>absenteeism, extra medication used, and (next) puncture under general<br /><br>anaesthesia.</p><br>