Effect of anesthetic ankle block, through local infiltration of medications Dexmedetomidine and Ropivacaine, for postoperative pain relief: a study with random selection of patients

Phase 4

Not yet recruiting

• Conditions: Postoperative Care; Hallux Valgus; Hammer Toe Syndrome; N02.421.585.722.700

• Registration Number: RBR-6yv2xry
• Lead Sponsor: Instituto Prevent Senior

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2021-06-29
• Study Completion: 2022-03-01
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Not yet recruiting
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion criteria are: adults undergoing foot surgery (hallux valgus correction, claw toes and tailor's bunion), of both genders, older than 18 years; having signed and agreed to the voluntary consent form to participate in the study (TCLE); not having a previous allergy or contraindication for the selected anesthetic procedure.

Exclusion Criteria

Exclusion criteria are: patients who are allergic to selected and offered anesthetic medications; refusal of the type of anesthetic procedure drawn and offered; anesthetic risk that contraindication is the type of anesthesia drawn and offered; patients with malignant tumors and infections present; patients with mental confusion or disoriented; patients under 18 years of age.

Study & Design

• Study Type: Intervention
• Study Design: Not specified