A study of post-extraction bleeding following warm saline mouth washes compared to no mouth washes during the 24 hours following surgery
| ISRCTN | ISRCTN30207928 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN30207928 |
| Protocol serial number | N0205153820 |
| Sponsor | Department of Health |
| Funders | Barts and The London NHS Trust (UK), NHS R&D Support Funding (UK) |
- Submission date
- 30/09/2005
- Registration date
- 30/09/2005
- Last edited
- 02/06/2017
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Oral Health
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year
Plain English summary of protocol
Not provided at time of registration
Contact information
Mr Z Abbasi
Scientific
Scientific
Ground Floor
Dental Institute
New Road
Whitechapel
London
E1 1BB
United Kingdom
| Phone | +44 (0)7803 496 050 |
|---|---|
| zubabb1@hotmail.com |
Study information
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| Scientific title | A study of post-extraction bleeding following warm saline mouth washes compared to no mouth washes during the 24 hours following surgery |
| Study objectives | 1. Does rinsing of the mouth after dental extractions of tooth induce excessive bleeding? 2. Are traditional post-extraction instructions evidence based? 3. To improve, simplify and validate post-operative instructions after tooth removal |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Dental extractions of tooth |
| Intervention | A randomised two-group study: 1. Warm saline mouth washes 2. No mouth wash |
| Intervention type | Other |
| Primary outcome measure(s) |
Absence/occurrence of bleeding over 24 hours. |
| Key secondary outcome measure(s) |
No secondary outcome measures |
| Completion date | 28/02/2005 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Not Specified |
| Sex | Not Specified |
| Target sample size at registration | 60 |
| Key inclusion criteria | 60 patients in two groups of 30 |
| Key exclusion criteria | Not provided at time of registration |
| Date of first enrolment | 29/11/2004 |
| Date of final enrolment | 28/02/2005 |
Locations
Countries of recruitment
- United Kingdom
- England
Study participating centre
Ground Floor
London
E1 1BB
United Kingdom
E1 1BB
United Kingdom
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|---|
| IPD sharing plan summary | Not provided at time of registration |
| IPD sharing plan |
Editorial Notes
02/06/2017: No publications found in PubMed, verifying study status with principal investigator
