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Morbidity associated with perioperative intravenous fluid in children undergoing tonsillectomy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN26015483
Enrollment
Unknown
Registered
2003-09-12
Start date
2001-11-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Ear, Nose and Throat: Tonsillectomy Ear, Nose and Throat Tonsillectomy

Interventions

Randomised controlled trial, patient, parent and ward nurses blinded to limb allocation, half the study group will receive a measured amount of intravenous fluid during the operation and half will not

Sponsors

Record provided by the NHS Trusts Clinical Trials Register - Department of Health (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Children aged between 2 and 15 years, both male and female undergoing tonsillectomy will be recruited.

Exclusion criteria

Exclusion criteria: Not provided at time of registration

Design outcomes

Primary

MeasureTime frame
The incidence and severity of vomiting, pain and activity disturbance will be monitored and recorded for 3 days post surgery.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

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