Clinical TrialID 8398

Efficacy of Topical Lidocaine/Prilocaine in Pain Management in Pleurocentesis

NCT05984264

Pleural Effusion

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Record Fields

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Clinical Trial Id
8398
Evidence Id
8398
Core Evidence Id
8398
Source Clinical Trial Id
8396
Herb2 Clinical Trial Id
HBCT008396
Nct Id
NCT05984264
Title
Efficacy of Topical Lidocaine/Prilocaine in Pain Management in Pleurocentesis
Status
Recruiting
Phase
Phase 4
Study Result
No
Study Condition
Pleural Effusion
Study Type
Interventional
Study Design
Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: NONE|Primary Purpose: TREATMENT
Intervention
DRUG: lidocaine 2.5% and prilocaine 2.5% cream in pain management before pleurocentesis.
Intervention Allocation
Non_Randomized
Intervention Model
Parallel
Intervention Mask
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
118
Outcome Measure
The severity of pain will be assessed using the visual analogue scale (VAS)., The severity of pain will be assessed using the visual analogue scale (VAS). The VAS consists of a 10cm line, with two endpoints representing 0 ('no pain') and 10 ('pain as bad as it could be'). Ask the patient to rate their current level of pain by placing a mark on the line. Use a ruler to measure the distance in centimeters from the 'no pain marker' (or zero) to the current pain mark. This provides a pain intensity score out of 10; for example, 6 out of 10 (or 6/10)., one day
Sponsor Collaborator
Assiut University
Funded By
OTHER
Location
Assuit University Hospital, Assiut, Assiut university 71515, Egypt
Other Id
BBBAAS
Start Date
2023-01-01
Primary Completion Date
2023-09
Completion Date
2023-12
First Posted
2023-08-09
Results First Posted
Last Update Posted
2023-08-09
Study Document
Study Url
https://clinicaltrials.gov/study/NCT05984264
Title Cn
Title En
Efficacy of Topical Lidocaine/Prilocaine in Pain Management in Pleurocentesis
Bilingual Status
semi_complete