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Evaluation of the efficacy of using LLLT on paresthesia

Evaluation of the efficacy of using LLLT on paresthesia recovery after implant surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240719062464N1
Enrollment
24
Registered
2024-10-06
Start date
2024-08-31
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Paraesthesia after implant surgery. Disorders of trigeminal nerve

Interventions

Intervention 1: Intervention group: After surgery and in the presence of paraesthesia, using a low-power diode laser with a wavelength of 805 to 1064 nm for each patient, 8 sessions of laser therapy i

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with paresthesia after implant surgery

Exclusion criteria

Exclusion criteria: Patients who do not want to have laser

Design outcomes

Primary

MeasureTime frame
Surface mechanical sensitivity. Timepoint: It is checked before the first laser therapy session and 2 weeks and 1 month after the last laser therapy session. Method of measurement: Virtual Analogue Scale.;Deep mechanical sensitivity. Timepoint: It is checked before the first laser therapy session and 2 weeks and 1 month after the last laser therapy session. Method of measurement: Virtual Analogue Scale.;Temperature sensitivity. Timepoint: It is checked before the first laser therapy session and 2 weeks and 1 month after the last laser therapy session. Method of measurement: Virtual Analogue Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMorteza Jalaiean nasrabadi

Mashhad University of Medical Sciences

JalaeianM971@mums.ac.ir+98 51 3859 4392

Outcome results

None listed

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