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Applying a 3D-printed device for pain relief associated with injection pain

Applying a 3D-printed device for pain relief associated with intradermal injection of local anesthesia: A randomized-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200057324
Enrollment
Unknown
Registered
2022-03-08
Start date
2022-03-15
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

pain

Interventions

Intervention group:Using disk
Control group:Routine brachial plexus anesthesia

Sponsors

Wuxi Ninth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients to undergo brachial plexus anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients who plan to undergo emergency surgery; 2. Persons under the age of 16; 3. Oral analgesics taken within 6 hours before surgery; 4. Patients with surgical history or local pain in the neck; 5. Communication barriers, unable to complete VAS and Likert scores; 6. Other local anesthesia contraindications.

Design outcomes

Primary

MeasureTime frame
VAS scores;—

Secondary

MeasureTime frame
Likert scores;—

Countries

Chian

Contacts

Public ContactMi Jingyi

Wuxi Ninth People's Hospital

1204549830@qq.com+86 15951519819

Outcome results

None listed

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