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A randomized controlled trial of subcutaneous tumescent-injection digital block versus traditional two injections dorsal digital block

A randomized controlled trial of subcutaneous tumescent-injection digital block versus traditional two injections dorsal digital block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003195
Enrollment
Unknown
Registered
2013-03-15
Start date
2013-05-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

digital trauma, digital tumor

Interventions

tumescent-injection group (group I):subcutaneous tumescent-injection digital block
traditional digital block (group II):traditional two injections dorsal digital block

Sponsors

The first affiliated hospital of Dalian medical university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients with digital trauma and digital tumor whose operation can be done during local digital anaesthesia; 2. Patients who are voluntary to participate this trial.

Exclusion criteria

Exclusion criteria: 1. patients with Lignocaine allergy; 2. Patients with peripheral neurovascular disorder, such as Raynaudd disease; 3. Previous digital replantation.

Design outcomes

Primary

MeasureTime frame
pain of initial pinprick on VAS;—

Secondary

MeasureTime frame
onset time of anaesthesia;failure rate;complication rate;—

Countries

China

Contacts

Public ContactLei Huang
huanglei2008@hotmail.com+86 18698652286

Outcome results

None listed

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