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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04846855
Other study ID # 2019-004504-35
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date October 14, 2020
Est. completion date April 14, 2022

Study information

Verified date February 2024
Source Ramsay Générale de Santé
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Peripheral loco-regional anesthesia (LRA) for anesthetic purposes is a technique widely used in adults for upper limb surgery. In pediatrics, LRA is not classically considered on its own. It is usually performed for analgesic purposes during sedation or general anesthesia. It is entirely possible to carry out awakened peripheral blocks in communicating children, of school age, thus avoiding the issues of GA in pediatrics, in particular in an emergency context. The use of Emla anesthetic skin patches for punctures (perfusion and LRA) as well as the viewing of cartoons on touch tablets during treatment can improve the perception of painless care such as LRA and treatment. In pediatrics, only ropivacaine at a concentration of 0.2% has Marketing Authorization in pediatrics in children under 12 for the production of peripheral blocks. On the basis of the experience of the Claude Galien Private Hospital in this area, it seems interesting to assess the feasibility of upper limb surgery under anesthetic LRA alone with a dose of ropivacaine at the concentration 0.35% in communicating children, of school age.


Description:

Peripheral loco-regional anesthesia (LRA) for anesthetic purposes is a technique widely used in adults for upper limb surgery. It allows peripheral surgeries to be performed without putting the patient to sleep and thus avoiding certain disadvantages of general anesthesia (GA). In pediatrics, LRA is not classically considered on its own. It is usually performed for analgesic purposes during sedation or GA. Subject to respecting a strict protocol and taking advantage of considerable developments in the field of LRA, it is entirely possible to carry out awakened peripheral blocks in communicating children, of school age, thus avoiding the pitfalls of GA in pediatrics, in particular in an emergency context (inhalation on a full stomach, respiratory risk in children with colds, inhalational anesthesia with an anxiety mask, postoperative vomiting nausea, disorientation and delusions upon waking ...) Indeed, the exclusive use of ultrasound, the use of adapted needles, the improvement of knowledge in sono-anatomy, the reduction in doses and concentrations of local anesthetics are all developments in the field of LRA allowing to improve the conditions of safety, comfort for the patient and success of the technique. Beyond technical considerations, there are ways to improve the child's experience with care. The use of Emla anesthetic skin patches for punctures (perfusion and ALR) as well as the viewing of cartoons on touch tablets during treatment can improve the perception of painless care such as ALR and treatment. charge in the operating room. In pediatrics, only ropivacaine at a concentration of 0.2% has Marketing Authorization in pediatrics in children under 12 for the production of peripheral blocks. Higher concentrations of ropivacaine, used in several pediatric studies, have nevertheless shown their good tolerance and their efficacy Under reserve not to exceed 3mg / kg and to use concentrations up to 0.5% On the basis of these arguments, and with the experience of the Claude Galien Private Hospital in this area, it seems interesting to assess the feasibility of upper limb surgery under anesthetic ALR alone with a dose of ropivacaine at the concentration 0.35% in communicating children, of school age.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date April 14, 2022
Est. primary completion date October 14, 2021
Accepts healthy volunteers No
Gender All
Age group 6 Years to 12 Years
Eligibility Inclusion Criteria: - Child aged 6 to 12. - Able to understand and express themselves. - Intended for orthopedic surgery of the upper limb involving the hand, wrist, forearm or elbow. - ASA class 1-2. - Patient who has given free and informed consent. - Parent present having given their free and informed consent. - Affiliated patient or beneficiary of a social security scheme Exclusion Criteria: - Refusal of the child and / or parent to participate in the study. - Immediate vital emergency. - Duration of planned surgery> 1h30. - History of allergy to LA. - Contraindication to carrying out ALR (local infection, pathology contraindicating ALR, preoperative neurological deficit). - Refusal by the surgeon. - Child already sedated or premedicated in the emergency room. - Digital tablet not available. - Patient participating in another clinical study.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
local anaesthetic injection
Realization by the anesthesiologist of the local anesthesia by single dose of ropivacaine 0.35% in perinervous under ultrasound with distraction by a tablette.

Locations

Country Name City State
France Hôpital Privé Claude Galien Quincy-sous-Sénart IDF

Sponsors (1)

Lead Sponsor Collaborator
Ramsay Générale de Santé

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary LRA success percentage of children in whom ALR and surgery were performed without additional sedation or general anesthesia. 2 hours
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