Study on treatment for dentin hypersensitivity

Study on treatment for dentin hypersensitivity - SzBvüZ

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00004663

Enrollment

120

Registered

2015-04-28

Start date

2015-09-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

dentin hypersensitivity

Interventions

Group 1: Experimental group receives hypnosis via mp3 for reduction of DHS. Patients are examined baseline, afte 1, 4 and 8 weeks. Group 2: Control group 1 receives Arginin-toothpaste for reduction o

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: healthy patients with dentin hypersensitivity (18-70 years), informed consent

Exclusion criteria

Exclusion criteria: - ongoing dental or periodontal tratment or treatment of the oral mucosa - insufficient oral hygiene - allergy against an ingredient of the study tooth paste - pregnancy or brast feeding - heavy mental disorders - intake of acidic drugs - Vegetarian or vegan - refulx disease

Design outcomes

Primary

Measure	Time frame
proof of reduction in dentin hypersensitivity by "Schiff Test" in 1, 4 and 8 weeks.	—

Secondary

Measure	Time frame
proof of reduction in dentin hypersensitivity by "Yeaple probe" after 1, 4 and 8 weeks.	—

Countries

Germany

Contacts

Public ContactJohan Wölber

Universität Freiburg, ZMK, Abt. f. Zahnerhaltungskunde und Parodontologie

johan.woelber@uniklinik-freiburg.de+49 (0) 761 270 47310

Outcome results

None listed

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