Comparison of clinical outcomes between conventional laparoscopic right hemicolectomy and single-incision laparoscopic right hemicolectomy in colon cancer trial
| ISRCTN | ISRCTN55622645 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN55622645 |
| Secondary identifying numbers | N/A |
- Submission date
- 07/02/2011
- Registration date
- 23/03/2011
- Last edited
- 23/03/2011
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Cancer
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 Weida Day
Scientific
Scientific
Department of Surgery
Kwong Wah Hospital
25 Waterloo Road
Hong Kong
00
Hong Kong
| weidaday@gmail.com |
Study information
| Study design | Prospective single-blind randomised controlled trial |
|---|---|
| Primary study design | Interventional |
| Secondary study design | Randomised controlled trial |
| Study setting(s) | Hospital |
| Study type | Treatment |
| Participant information sheet | Not available in web format, please use the contact details below to request a patient information sheet |
| Scientific title | Comparison of clinical outcomes between conventional laparoscopic right hemicolectomy and single-incision laparoscopic right hemicolectomy in colon cancer: A randomised controlled trial. |
| Study objectives | To study if patients with single-inicison laparoscopic right hemicolectomy have less post-operative pain. |
| Ethics approval(s) | Kowloon West Cluster Clinical Research Ethic Committee, Hospital Authority approved on 15th September 2010 |
| Health condition(s) or problem(s) studied | Carcinoma of colon (right colon) |
| Intervention | Laparoscopic right hemicolectomy and single-incision laparoscopic right hemicolectomy |
| Intervention type | Other |
| Primary outcome measure | Wound pain-using visual analog scale and it will be carried out from post-op Day 1 to Day 7 |
| Secondary outcome measures | 1. Morbidity- will be short term complication e.g. bleeding, infection, collection, reoperation 2. Hosptial stay 3. Survival-follow-up patient for 5 years with regular follow-up, then analyze the survival rate |
| Overall study start date | 01/10/2010 |
| Completion date | 01/10/2012 |
Eligibility
| Participant type(s) | Patient |
|---|---|
| Age group | Adult |
| Sex | Both |
| Target number of participants | 100 |
| Key inclusion criteria | Colon cancer involving: 1. Caecum 2. Ascending colon 3. Hepatic flexure 4. Proximal transverse colon |
| Key exclusion criteria | 1. Tumour invades other organ 2. Tumour larger than 6cm 3. Patients with intestinal obstruction 4. Patients refused study or cannot understand the study 5. Children 6. Pregnant women 7. Mental retarded patients |
| Date of first enrolment | 01/10/2010 |
| Date of final enrolment | 01/10/2012 |
Locations
Countries of recruitment
- Hong Kong
Study participating centre
Department of Surgery
Hong Kong
00
Hong Kong
00
Hong Kong
Sponsor information
Kwong Wah Hospital, Hospital Authority (Hong Kong)
Hospital/treatment centre
Hospital/treatment centre
Department of Surgery
Kwong Wah Hospital
c/o Weida Day
25 Waterloo Road, Kowloon
Hong Kong
00
Hong Kong
| Phone | +852 35178090 |
|---|---|
| weidaday@gmail.com | |
"ROR" |
https://ror.org/03s9jrm13 |
Funders
Funder type
Hospital/treatment centre
Kwong Wah Hospital, Hospital Authority (Hong Kong)
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 |
