Heavy prilocaine versus heavy bupivacaine for early patient mobility in perianal day-case surgery: A randomized double-blind clinical trial

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

PACTR

Registry ID

PACTR202412590651592

Enrollment

Registered

2024-12-03

Start date

2023-07-01

Completion date

Unknown

Last updated

2026-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anaesthesia

Interventions

Bupivacaine Group

Prilocaine Group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: age 18-60 years body mass index of 20-35 height of 150-175 cm American Society of Anesthesiologists physical status I or II

Exclusion criteria

Exclusion criteria: known allergy to local anesthetics any standard contraindications to neuraxial block

Design outcomes

Primary

Measure	Time frame
time taken for patients to walk unaided	—

Secondary

Measure	Time frame
time to first micturition;time to first postoperative analgesia;incidence of postoperative nausea and vomiting	—

Countries

Egypt

Contacts

Public ContactIslam Hamed

Associate professor of Anesthesia Faculty of Medicine Ain Shams University

islamgamalhamed@gmx.com00000000000

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Feb 4, 2026