Skip to content

Pain Assessment of the IVF Needle

Pain Assessment of the IVF Needle - PAIN

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON47399
Enrollment
93
Registered
2016-06-08
Start date
2017-02-16
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

involuntary childlessness Subfertility

Interventions

A transvaginal ultrasound-guided puncture with the Sense OD 20/17 Gauge needle or a transvaginal ultrasound-guided puncture with the Origio 14 Gauge needle for ovum pick up.

Sponsors

Jeroen Bosch Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Indication for IVF/ICSI - Female age between 18 and 42 years - Informed consent - Normal position of the ovaries

Exclusion criteria

Exclusion criteria: - A previous IVF or ICSI treatment - Endometriosis - BMI > 35 - Use of painmedication - OHSS - Operation in lower abdomen

Design outcomes

Primary

MeasureTime frame
Primarily there will be a look at the difference in pain scores with the use of a thinner needle.

Secondary

MeasureTime frame
Secondary outcomes were differences in: oocyte quality, total procedure time, follow procedure/fertilization, demand for additional analgesia during the procedure, time to resign after puncture, pain medication days after puncture, possible influence of age and/or weight on pain score, relationship between pain score and indication puncture, impact doctor performing puncture on pain score and whether the *overall* savings for the economy, considering absenteeism, extra medication used, and (next) puncture under general anaesthesia.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)