A comparative, double blind trial between'older' and 'newer' local anesthetics in forefoot surgery under echographic popliteal block.

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2007-004936-22-BE

Enrollment

Registered

2007-10-12

Start date

2007-10-29

Completion date

Unknown

Last updated

2021-11-29

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

Conditions

Regional anesthesia strategies during forefoot surgery.

Interventions

Trade Name: Naropin Pharmaceutical Form: Injection* INN or Proposed INN: ROPIVACAINE CAS Number: 84057954 Concentration unit: mg/ml milligram(s)/millilitre Concentration type: equal Concentration numb

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - subjects scheduled for elective forefoot 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 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: - Chronic pain patient. - Known allergy for local anesthetics or polyallergic diathesis. - < 18 years of age.

Design outcomes

Primary

Measure	Time frame
Main Objective: 1. To compare the time needed before sensor/motor block occurs 2. To compare the level of peroperative anesthesia.;Secondary Objective: ;Primary end point(s):	—

Countries

Belgium

Outcome results

None listed

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