Informations générales (source: ClinicalTrials.gov)
Effect of Tourniquet Abstention on Pain Reduction in Venous Sampling in the Elderly People : Randomized Trial (NO-GARROT)
Interventional
N/A
Hôpital NOVO (Voir sur ClinicalTrials)
mai 2022
novembre 2024
21 septembre 2024
This prospective study evaluates the effect of abstaining from tourniquets on pain
reduction during the venous puncture of the elderly people.
Etablissements
| Les établissements d'Île-de-France ayant mis à jour leurs données Origine et niveau de fiabilité des données | |||||
|---|---|---|---|---|---|
| HOPITAL NOVO | VELLA QUILLIEN | 04/12/2024 13:04:50 | Contacter | ||
| Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| AP-HP - Hôpital Louis Mourier | Douma ATHENA | Contact (sur clinicalTrials) | |||
| CHI DE CRETEIL | Caroline Legal | Contact (sur clinicalTrials) | |||
| Les établissements sans correspondance certaine dans le répertoire FINESS dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
| Geriatric Department - CH Cholet - 49 300 - Cholet - France | Tiphaine RETAILLEAU | Contact (sur clinicalTrials) | |||
| Geriatric Department - CHRU Brest - 29600 - Brest - France | Contact (sur clinicalTrials) | ||||
Critères
Tous
Inclusion Criteria:
- ≥ 75 years and over,
- Hospitalized in internal medicine or geriatric department,
- For which the 2 upper limbs are accessible to venous puncture (due to the multiple
attempts that may be necessary to take a sample during the hospitalization),
- For which at least one vein is visible or palpable on an upper limb,
- Without venous puncture since admission in the department,
- Patient who did not receive a topical anesthetic before the venous puncture (Emla
type)
- Communicating patient, able to assess their pain on a digital scale,
- Patients with affiliation to a social security system or beneficiary ,
- Written informed consent (IC) obtained.
- ≥ 75 years and over,
- Hospitalized in internal medicine or geriatric department,
- For which the 2 upper limbs are accessible to venous puncture (due to the multiple
attempts that may be necessary to take a sample during the hospitalization),
- For which at least one vein is visible or palpable on an upper limb,
- Without venous puncture since admission in the department,
- Patient who did not receive a topical anesthetic before the venous puncture (Emla
type)
- Communicating patient, able to assess their pain on a digital scale,
- Patients with affiliation to a social security system or beneficiary ,
- Written informed consent (IC) obtained.
- Patient already included,
- Previous pain localized to the upper limbs,
- Hematoma at the planned site of skin-vascular breakage,
- Hemiplegic or quadriplegic patient,
- Patient with lymphedema in the upper limbs,
- Patient with behavioral disorders that may interfere with the proper functioning of
the sampling,
- Patient with cognitive impairment preventing understanding of the study and adequate
assessment pain (CODEX cognitive score of category C or D),
- Patient placed under legal protection (guardianship).