Haloperidol as an antiemetic following abdominal hysterectomy - a comparison with Zofran®
| ISRCTN | ISRCTN21871435 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN21871435 |
| Secondary identifying numbers | N0558111116 |
- Submission date
- 12/09/2003
- Registration date
- 12/09/2003
- Last edited
- 17/09/2012
- Recruitment status
- Stopped
- Overall study status
- Stopped
- Condition category
- Surgery
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
Dr Andrew White
Scientific
Scientific
Milton Keynes General NHS Trust
Standing Way
Eaglestone
Milton Keynes
MK6 5LD
United Kingdom
| Phone | +44 (0)1908 660033 |
|---|---|
| andrew.white@mkgeneral.nhs.uk |
Study information
| Study design | Randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Scientific title | |
| Study objectives | Following withdrawal of Droperidol can Haloperidol, which has been used in palliative care, give good antiemetic effect following acute surgery? |
| Ethics approval(s) | Not provided at time of registration |
| Health condition(s) or problem(s) studied | Post operative antiemetics |
| Intervention | Prospective randomised trial. 17/09/2012: Please note that this trial was stopped as the trial objectives were no longer viable |
| Intervention type | Drug |
| Pharmaceutical study type(s) | |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Haloperidol, ondansetron (Zofran®) |
| Primary outcome measure | Not provided at time of registration |
| Secondary outcome measures | Not provided at time of registration |
| Overall study start date | 01/10/2001 |
| Completion date | 30/09/2003 |
| Reason abandoned (if study stopped) | Objectives no longer viable |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Female |
| Target number of participants | Not provided at time of registration |
| Key inclusion criteria | All American Society of Anesthesiologists (ASA) I - III females undergoing abdominal hysterectomy who give their consent. |
| Key exclusion criteria | Does not match inclusion criteria |
| Date of first enrolment | 01/10/2001 |
| Date of final enrolment | 30/09/2003 |
Locations
Countries of recruitment
- England
- United Kingdom
Study participating centre
Milton Keynes General NHS Trust
Milton Keynes
MK6 5LD
United Kingdom
MK6 5LD
United Kingdom
Sponsor information
Department of Health (UK)
Government
Government
Richmond House
79 Whitehall
London
SW1A 2NL
United Kingdom
| Website | http://www.doh.gov.uk |
|---|
Funders
Funder type
Hospital/treatment centre
Milton Keynes General NHS Trust (UK)
No information available
Results and Publications
| Intention to publish date | |
|---|---|
| Individual participant data (IPD) Intention to share | No |
| IPD sharing plan summary | Not provided at time of registration |
| Publication and dissemination plan | Not provided at time of registration |
| IPD sharing plan |
