Vibrational anesthesia while having a contraceptive implant

The efficacy of vibrational anesthesia for reducing pain and anxiety in a group receiving a contraceptive implant: A single-blinded randomized controlled trial

Status

Unknown

Phases

Phase 2Phase 3

Study type

Interventional

Source

TCTR

Registry ID

TCTR20230217006

Enrollment

Registered

2023-02-17

Start date

2023-02-15

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

Pain and anxiety during contraceptive implantation Vibration anesthesia Contraceptive implant Pain Anxiety

Interventions

The experimental group will receive a contraceptive implant with vibration anesthesia. Vibration Anesthesia Device (VAD) from Blaine Labs which is approved by the US FDA will be used for the purpos

Experimental Procedure/Surgery,No Intervention Procedure/Surgery

Vibration Anesthesia,Controls

Eligibility

Sex/Gender

Female

Age

18 Years to 49 Years

Inclusion criteria

Inclusion criteria: Women who will be receiving their first contraceptive implantation

Exclusion criteria

Exclusion criteria: Women who already have a contraceptive implant

Design outcomes

Primary

Measure	Time frame
Pain immediately after the procedure Numeric rating scale	—

Secondary

Measure	Time frame
Anxiety immediately after the procedure The State Anxiety Inventory (STAI) Form Y	—

Countries

Thailand

Contacts

Public ContactNamphung Nanthawong

Chaiyaphum Hospital

honey_md@hotmail.com0832877331

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026