A dosing study with the anesthetic prilotekal for spinal anesthesia during day care surgery.

Phase 1

• Conditions: spinal anesthesia for open inguinal hernia repair or lower limb surgery; MedDRA version: 18.1Level: LLTClassification code 10041538Term: Spinal anesthesiaSystem Organ Class: 100000004865; Therapeutic area: Analytical, Diagnostic and Therapeutic Techniques and Equipment [E] - Anesthesia and Analgesia [E03]

• Registration Number: EUCTR2015-000882-29-NL
• Lead Sponsor: Reinier de Graaf Groep

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-02-17
• Last Update Posted: 3 November 2020

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 130

Inclusion Criteria

patients 18 year and older planned for spinal anesthesie in day case surgery
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 100
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 30

Exclusion Criteria

pregnancy
allergy to prilocaine

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified