Haloperidol as an antiemetic following abdominal hysterectomy - a comparison with Zofran®
| ISRCTN | ISRCTN21871435 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN21871435 |
| Protocol serial number | N0558111116 |
| Sponsor | Department of Health (UK) |
| Funder | Milton Keynes General NHS Trust (UK) |
- 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
| Primary study design | Interventional |
|---|---|
| Study design | Randomised controlled trial |
| Secondary study design | Randomised controlled trial |
| 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 |
| Phase | Not Specified |
| Drug / device / biological / vaccine name(s) | Haloperidol, ondansetron (Zofran®) |
| Primary outcome measure(s) |
Not provided at time of registration |
| Key secondary outcome measure(s) |
Not provided at time of registration |
| Completion date | 30/09/2003 |
| Reason abandoned (if study stopped) | Objectives no longer viable |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Female |
| 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
- United Kingdom
- England
Study participating centre
Milton Keynes General NHS Trust
Milton Keynes
MK6 5LD
United Kingdom
MK6 5LD
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 |
