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The influence of improved disassembly operation on the pain of inpatients with video electroencephalogram

The influence of improved disassembly operation on the pain of inpatients with video electroencephalogram

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500105113
Enrollment
Unknown
Registered
2025-06-30
Start date
2025-07-01
Completion date
Unknown
Last updated
2025-07-07

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

Conditions

Epilepsy

Interventions

Experimental Group A and Group C:The content of the disassembly operation in the experimental group: On the basis of the control group, a waterproof head cap was used to surround the patients head, an
Control Group B and Group D:The operation content of the control group getting off the machine: Only the conventional operation was used, that is, getting off the machine by hand tearing off the adhes

Sponsors

The Seventh Affiliated Hospital, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 17 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Patients who need to undergo video electroencephalogram (EEG) examinations in our department tend to have stable conditions 2. Patients aged 6 to 17 years (children's group 6-12 years old, adolescent group 13-17 years old) 3. The patient is conscious and the family members can cooperate to observe and record the questionnaire 3. No participation in other clinical studies within 3 months 5. No adverse events occurred 6. Agree to participate in this research

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Patients not monitored by video electroencephalogram 2. Patients aged less than 6 years or 18 years or older 3. Patients who are unable to cooperate with the observation record questionnaire (those with language or consciousness disorders, severe cognitive or mental disorders, unstable or deteriorating conditions) 4. Patients who do not agree to participate in this study

Design outcomes

Primary

MeasureTime frame
Pain scale score;

Secondary

MeasureTime frame
Hospitalization satisfaction;

Countries

China

Contacts

Public ContactFanli Zeng

The Seventh Affiliated Hospital, Sun Yat-sen University

zengfanli@sysush.com+86 185 7730 9685

Outcome results

None listed

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