Trials / Unknown
UnknownNCT02590705
Anesthesia Lumbar Puncture In Children
Anesthesia Lumbar Puncture In Children (ALPIC)
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Beijing Children's Hospital · Academic / Other
- Sex
- All
- Age
- 1 Month – 18 Years
- Healthy volunteers
- Not accepted
Summary
The study is carried out in a prospectively randomly controlled way. In the context of acknowledgement and understanding from parents, by comparing with traditional process(no anesthesia), lidocaine surface anesthesia is randomly selected. All children will be evaluated by the FLACC (The face, legs, activity, cry, consolability behavioral tool) scale to quantitatively assess degree of pain during lumbar puncture. Time and success rate of the lumber puncture will be recorded and analyzed. A questionnaire about bad memory during lumbar puncture for all parents and children will be investigated in order to establish an optimized lumbar puncture management process.
Detailed description
The purpose of this study is to establish an optimized lumbar puncture management process on the basis of fully understanding of parents and children. An improved process consisting of painless lumbar puncture (LP) and comfortable LP will be established upon completion of this study.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine | surface anesthesia with lidocaine |
Timeline
- Start date
- 2015-10-01
- Primary completion
- 2016-09-01
- Completion
- 2016-09-01
- First posted
- 2015-10-29
- Last updated
- 2015-10-29
Source: ClinicalTrials.gov record NCT02590705. Inclusion in this directory is not an endorsement.