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Clinical study on the treatment and outcome of dry socket

Clinical study on the treatment and outcome of dry socket

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100050055
Enrollment
Unknown
Registered
2021-08-16
Start date
2021-08-10
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Dry Socket

Interventions

Rinse dressing change Group:No
New drugs Group:No

Sponsors

Hospital of Stomatology, Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients who were diagnosed with dry socket in the oral surgery clinic of our hospital; 2. Aged 18-70 years.

Exclusion criteria

Exclusion criteria: 1. Patients with systemic diseases and mental diseases; 2. Patients who are pregnant or planning to become pregnant, lactating or menstruating; 3. Patients with residual tooth roots or serious maxillofacial space infection in the extraction wound after tooth extraction; 4. Patients who are treated with antibiotics within one week after the onset of the disease, or those who need antibiotics for systemic infections; 5. Other cases deemed unsuitable for inclusion by the investigator.

Design outcomes

Primary

MeasureTime frame
Pain relief time;

Countries

China

Contacts

Public ContactSun Rui

Hospital of Stomatology, Wuhan University

sunrui12@whu.edu.cn+86 27 87686386

Outcome results

None listed

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