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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03854604
Other study ID # N-110-2018
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 20, 2019
Est. completion date September 20, 2019

Study information

Verified date August 2020
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

It has been demonstrated that infants and children experience pain in a similar manner to adults, however it used to be undertreated when compared to adult.

Perfusion Index (PI) derived from pulse plethysmography waveform, represents a ratio of pulsatile signal (during arterial inflow) to non-pulsatile signal. PI can represent the peripheral perfusion dynamics due to change of peripheral vasomotor tone. Low PI values suggest peripheral vasoconstriction and high PI values suggest peripheral vasodilation.

The sympathetic nervous system is inherently involved in the pathophysiological responses evoked by painful stimulation.

In the current study, investigators hypothesise that the PI could be a good objective tool for assessment of postoperative pain in children undergoing adenotonsillectomy.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date September 20, 2019
Est. primary completion date June 20, 2019
Accepts healthy volunteers No
Gender All
Age group 3 Years to 7 Years
Eligibility Inclusion Criteria:

1. ASA physical status I-II

2. Age 3 to 7 years

3. Children undergoing adenotonsillectomy.

Exclusion Criteria:

1. Parents' refusal.

2. Children with behavioral changes

3. Children with physical developmental delay

4. Children on treatment with sedative or anticonvulsant.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
postoperative pain assessment
evaluation of the efficacy of PI as an objective measure for postoperative pain assessment in pediatric population undergoing adenotonsillectomy.

Locations

Country Name City State
Egypt Abeer Ahmed Cairo
Egypt Anesthesia department - Faculty of medicine- Cairo University Cairo
Egypt Kasr Alainy Faculty of Medicine - Cairo university Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between postoperative (Children's Hospital of Eastern Ontario Scale ) CHEOPS score and postoperative perfusion index. the time span between arrival to PACU and for at least two hours postoperative
Secondary validity of perfusion index to predict postoperative pain and the need of rescue analgesia he time span between arrival to PACU and for at least two hours postoperative
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