Skip to content

Open versus specific questioning to assess pain during anaesthetic follow-up after caesarean birth: a randomised trial

Open versus specific questioning to assess pain during anaesthetic follow-up after caesarean birth: a randomised trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000121268
Enrollment
250
Registered
2009-02-19
Start date
2009-01-01
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The primary purpose of this study is to determine whether the perception of pain is affected by the way women are questioned after their caesarean birth

Interventions

On the postoperative anaesthetic review round within 12-72 hours of the surgery, all Women allocated to open questioning will be asked how they are feeling followed within 5 minutes by the closed question of whether they are comfortable. If they have not already that they have pain, they will then immediately be asked whether they have pain or not and how severe is their pain. This will be measured using a ten point Verbal Numerical Rating Score (VNRS) with zero being no pain while 10 is the wor

On the postoperative anaesthetic review round within 12-72 hours of the surgery, all Women allocated to open questioning will be asked how they are feeling followed within 5 minutes by the closed question of whether they are comfortable. If they have not already that they have pain, they will then immediately be asked whether they have pain or not and how severe is their pain. This will be measured using a ten point Verbal Numerical Rating Score (VNRS) with zero being no pain while 10 is the worst pain imaginable. Those women allocated to closed questioning will be asked whether they are in pain and to score the pain first prior to then being asked (within 5 minutes) how they are feeling.

Sponsors

Women's and Children's Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

within 72 hour of their caesarean section

Exclusion criteria

women requiring a translator and those with intellectual impairment

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026