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Electronic continuous pain measurement versus Verbal Rating Scale in gynaecology

Electronic continuous pain measurement versus Verbal Rating Scale in gynaecology: a prospective observational cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN15427669
Enrollment
108
Registered
2017-01-30
Start date
2011-08-01
Completion date
Unknown
Last updated
2017-02-20

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

Conditions

Gynaecological procedures Urological and Genital Diseases Gynaecological procedures

Interventions

Before the procedure, patients have their anxiety score recorded. When the patient is positioned, she receives instructions on the use of the CPSM and as a part of this instruction the meter is tested

Sponsors

VU University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Aged between 18-80 years 2. Scheduled for a hysteroscopy, colposcopy or ovum pick-up in an outpatient setting

Exclusion criteria

Exclusion criteria: 1. Inability to comprehend Dutch or English properly 2. For hysteroscopy: pregnancy or women in the luteal phase without the use of contraception, known cervical stenosis or malignancy, current Sexual Transmitted Disease (STD) or Pelvic Inflammatory Disease (PID) or contra-indications for the use of NSAIDs

Design outcomes

Primary

MeasureTime frame
Pain of outpatient gynecological procedure is measured using the Verbal Rating Scale (VRS 0-10) directly after a procedure versus pain measurement and using the Continuous Pain Score Meter (CPSM, CPSM-AUC, CPSM-PPS, CPSM-APS) during the procedure.

Secondary

MeasureTime frame
1. Recollection of pain perception is assessed using the Verbal Rating Scale (VRS 0-10) after two years 2. Anxiety is measured using a numerical rating scale (0-10) at baseline 3. Tolerability of the procedure is assessed post-surgery and after two years

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026