HemorrhoidsNCT00503269
Local Anaesthetic Day-care Haemorrhoidectomy Challenges Traditional Concepts - a Randomised Controlled Trial
A study testing Hemorrhoidectomy in people with Hemorrhoids, run by East Kent Hospitals University NHS Foundation Trust at 1 site in United Kingdom.
Trial summary
Background: Local anaesthetic day-care open haemorrhoidectomy (LH) is feasible, cheap and may be the cost-effective surgical approach to third degree haemorrhoids. This prospective randomised controlled trial compares patient's evaluation of LH with general anaesthetic day-care Park's modified Milligan-Morgan… Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Hemorrhoids
- What is being tested?
- Hemorrhoidectomy
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 42 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- Jul 2005to Jul 2007
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Third degree haemorrhoids
Who cannot join
- Unfit for day-surgery or general anaesthesia.
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Cost Effectiveness of Local Anaesthetic Day Surgical Haemorrhoidectomy
Background: Local anaesthetic day-care open haemorrhoidectomy (LH) is feasible, cheap and may be the cost-effective surgical approach to third degree haemorrhoids. This prospective randomised controlled trial compares patient's evaluation of LH with general anaesthetic day-care Park's modified Milligan-Morgan haemorrhoidectomy (GH).
Methods: 41 patients with third degree haemorrhoids were randomised to LH (19 cases) and GH (22 cases). Demographics were comparable. Independent assessment (by a research nurse) and clinical evaluation ran parallel for 6 months. Outcome measures were average and expected pain scores for 10 days; satisfaction scores at 10 days, 6 weeks and 6 months. Secondary outcomes were journey time and cost in day surgery.
Read the detailed description
INTRODUCTION:
Open haemorrhoidectomy is a commonly performed painful operation. In 1998-99, 26514 haemorrhoidectomies were performed in the UK of which 14373 were day cases. A further 5342 could have been performed as day surgery1. Improvements in multimodal2 and pre-emptive analgesia3, introduction of stapled anopexy4 and improvements in patient counselling5 have led to increasing number of day surgical treatment of haemorrhoids. Technique of LH is described6-11 but with the paucity of randomised controlled trials this is rarely offered as a routine choice to patients with third degree haemorrhoids.
AIM:
This randomised controlled trial compares patient-evaluation of postoperative pain and expected pain scores for 10 days and satisfaction scores at 10 days, 6 weeks and 6 months between local and general anaesthetic day surgical open haemorrhoidectomy. Clinical outcomes (for 6 months), cost comparison and evaluation of total journey time in day surgical unit formed part of the study.
PATIENTS AND METHODS:
This randomised controlled trial was approved by the Research and Development department and the Local Research Ethics committee. We performed a pilot evaluation of ten-day average pain and expectation scores after LH in 7 patients. Based on the data from this pilot study and the average pain scores from the literature for GH, we calculated a requirement of 40 patients to give a 90% power to the study at the 5% significance level (student's t-test) to detect a 22% difference in 10 day average pain scores with a standard deviation of 1.712. Null hypothesis was that there was no difference in the pain scores between the two groups.
Forty two patients with third degree haemorrhoids had full explanation of the trial (verbal and written with copies sent to their GP) and were randomised [Figure 1] on the day of surgery after consent. Patients unfit for day-surgery were excluded. Computer generated random numbers with opaque envelopes [produced by the principal researcher (GNR)] were opened by the research nurse (WH) after obtaining the research consent.
Verbal and written information of the expected postoperative course following open haemorrhoidectomy were given to all patients. This leaflet detailed the measures to take in the event of constipation or difficulty in passing urine, if such a problem arose. They were given the research nurse's contact number, in the event of a problem and were advised to contact out-of-hours GP service or the research nurse.
Research nurse [WH] assessed their pain and expectation scores in the post operative period on the day of surgery and spoke to all the patients on the day after surgery to record their comments and reinforce the importance of accurate scoring. Patients then recorded their pain and expectation scores at home for 10 days. This was the average of the pain that the patients experienced before, during and after defecation or the average of the pain during the course of the day. Two patients failed to return their 10 day pain scores [7%].
Pain scores were recorded on a ten-point Visual-analogue scale with scores from 1 to 10, with 1 being 'no pain' and 10 being 'as bad as it could be'. Ten-point patient expectation score was -5 to 5 with -5 being 'much better than expected' and 5 being 'much worse than expected'. Seven point satisfaction score was -3 to 3 with -3 being 'extremely dissatisfied' and 3 being 'extremely satisfied'.
Clinical follow-up by the surgeon (NGR) at 10 days, 6 weeks and 6 months evaluated the surgical outcome and recorded all surgical complications. Patients sent their satisfaction scores directly to the research nurse at these time-points and were un-influenced by the surgical out-patient visit.
All haemorrhoidectomies [Park's modified Milligan-Morgan technique13] were performed by a single surgeon [NGR]. Prone-Jacknife position (with buttocks strapped apart) was used for those randomised to local anaesthesia while Lithotomy-Trendelenburg position was used for those undergoing the procedure under general anaesthesia. Those with Type B and C buttocks10 needed more Trendelenburg position.
Perianal block was used for all patients irrespective of their randomisation. GH were given the block prior to commencement of surgery. This was performed with 20 ml of 1% Lignocaine (with 1 in 10000 Adrenaline) injected at four sites [midline anterior and posterior; left and right lateral], fanning the needle in three directions at each of the four sites; care being taken to inject outside the external sphincter, to avoid pain. Once the sphincter muscle relaxed with the perianal block, a further 10 ml of the same anaesthetic was injected submucosally raising a bleb in each of sites corresponding to the sites of perianal block. This bleb was massaged inferiorly. No sedation was used with local anaesthetic haemorrhoidectomy.
Following diathermy excision of haemorrhoids, a tube of lignocaine gel (Instillagel) was instilled into the anal canal followed by insertion of a gram of metronidazole and 50 mg of voltarol unless a history of asthma contraindicated the use of Voltarol in which case that was omitted. A soft sponge 'pack' [curisponge] was subsequently inserted. Patients were warned pre-operatively to expect the passage of the gelatinous curisponge in the post-operative period with their first defaecation.
A package of medications was given to take home (TTA). TTA contained Co-codamol, Ibuprofen, Metronidazole, Lactulose, Dulcolax, 5% lignocaine ointment and 2% Diltiazem cream, with detailed instructions on its usage. Message in the post-operative instruction leaflet was reiterated prior to discharge.
Journey time was calculated as the time elapsed between the start of anaesthesia and patient going home.
Infection was defined as presence of purulent discharge with heightened pain, a visit to their general practitioner and use of antibiotics over and above the Metronidazole prescribed on discharge.
Sum of the individual costs of the suture material, anaesthesia, cost of day surgery staff, recovery room costs and post operative medications were the basis of cost analysis.
Statistical analysis:
Data collected on Microsoft Excel was analysed on 'Analyse-it for Microsoft Excel' [Analyse-it Software Ltd, Leeds, UK]. Chi-square test and Mann-Whitney U test were used. Where the data was normally distributed as in the comparison of age, student's t-test was used. Serial measurements on linear analogue pain score were summarised by calculating the average pain over the 10-day time period for each patient as a summary measure14.
- Conditions
- Hemorrhoids
- Being tested
- Hemorrhoidectomy
- Keywords
- Haemorrhoidectomy, Local anaesthesia
- Medical subject headings
- Hemorrhoids
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HemorrhoidectomyProcedure or surgery
Hemorrhoidectomy under local anaesthesia
HemorrhoidectomyProcedure or surgery
General anaesthetic haemorrhoidectomy
| Study group | Role | What they receive |
|---|---|---|
| 1 | Active comparator | 30 ml of 1% Lignocaine with 1:10,000 Adrenaline Receives: Procedure: Hemorrhoidectomy |
| 2 | Active comparator | Standard General anaesthesia with Enflurane and Propofol. Receives: Procedure: Hemorrhoidectomy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Average pain and expectation score.
Measured: 6 months
Secondary outcomes (1)
Journey time and cost analysis
Measured: 6 months.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Jul 2007 (estimated)
- Study startJul 2005
- Primary completionJun 2007
- Study completionJul 2007
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for HemorrhoidsStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 42 participants (actual)
Sponsor and investigators
- Lead sponsor
- East Kent Hospitals University NHS Foundation Trust
- Sponsor type
- Other government
- Responsible party
- Sponsor
- Investigators
- Nagesh G Rao, FRCS, MD, Principal investigator, East Kent NHS Trust
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00503269
- Sponsor's protocol ID
- AA/dd
- Status last verified
- Sep 2023
- First submitted
- 16 Jul 2007
- Last updated
- 14 Sep 2023
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Kushwaha R, Hutchings W, Davies C, Rao NG. Randomized clinical trial comparing day-care open haemorrhoidectomy under local versus general anaesthesia. Br J Surg. 2008 May;95(5):555-63. doi: 10.1002/bjs.6113.
PubMed 18389499
Study at a glance
From the registry record, last updated by the sponsor on 14 Sep 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Cost Effectiveness of Local Anaesthetic Day Surgical Haemorrhoidectomy
- ClinicalTrials.gov ID
- NCT00503269
- Acronym / sponsor ID
- AA/dd
- Conditions
- Hemorrhoids
- Keywords
- Haemorrhoidectomy, Local anaesthesia
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 42 participants (actual)
- Lead sponsor
- East Kent Hospitals University NHS Foundation TrustOther government
- Study start
- Jul 2005
- Primary completion
- Jun 2007 (actual)
- Study completion
- Jul 2007 (actual)
- First posted
- 18 Jul 2007 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Background: Local anaesthetic day-care open haemorrhoidectomy (LH) is feasible, cheap and may be the cost-effective surgical approach to third degree haemorrhoids. This prospective randomised controlled trial compares patient's evaluation of LH with general anaesthetic day-care Park's modified Milligan-Morgan haemorrhoidectomy (GH).
Methods: 41 patients with third degree haemorrhoids were randomised to LH (19 cases) and GH (22 cases). Demographics were comparable. Independent assessment (by a research nurse) and clinical evaluation ran parallel for 6 months. Outcome measures were average and expected pain scores for 10 days; satisfaction scores at 10 days, 6 weeks and 6 months. Secondary outcomes were journey time and cost in day surgery.
Detailed description
INTRODUCTION:
Open haemorrhoidectomy is a commonly performed painful operation. In 1998-99, 26514 haemorrhoidectomies were performed in the UK of which 14373 were day cases. A further 5342 could have been performed as day surgery1. Improvements in multimodal2 and pre-emptive analgesia3, introduction of stapled anopexy4 and improvements in patient counselling5 have led to increasing number of day surgical treatment of haemorrhoids. Technique of LH is described6-11 but with the paucity of randomised controlled trials this is rarely offered as a routine choice to patients with third degree haemorrhoids.
AIM:
This randomised controlled trial compares patient-evaluation of postoperative pain and expected pain scores for 10 days and satisfaction scores at 10 days, 6 weeks and 6 months between local and general anaesthetic day surgical open haemorrhoidectomy. Clinical outcomes (for 6 months), cost comparison and evaluation of total journey time in day surgical unit formed part of the study.
PATIENTS AND METHODS:
This randomised controlled trial was approved by the Research and Development department and the Local Research Ethics committee. We performed a pilot evaluation of ten-day average pain and expectation scores after LH in 7 patients. Based on the data from this pilot study and the average pain scores from the literature for GH, we calculated a requirement of 40 patients to give a 90% power to the study at the 5% significance level (student's t-test) to detect a 22% difference in 10 day average pain scores with a standard deviation of 1.712. Null hypothesis was that there was no difference in the pain scores between the two groups.
Forty two patients with third degree haemorrhoids had full explanation of the trial (verbal and written with copies sent to their GP) and were randomised [Figure 1] on the day of surgery after consent. Patients unfit for day-surgery were excluded. Computer generated random numbers with opaque envelopes [produced by the principal researcher (GNR)] were opened by the research nurse (WH) after obtaining the research consent.
Verbal and written information of the expected postoperative course following open haemorrhoidectomy were given to all patients. This leaflet detailed the measures to take in the event of constipation or difficulty in passing urine, if such a problem arose. They were given the research nurse's contact number, in the event of a problem and were advised to contact out-of-hours GP service or the research nurse.
Research nurse [WH] assessed their pain and expectation scores in the post operative period on the day of surgery and spoke to all the patients on the day after surgery to record their comments and reinforce the importance of accurate scoring. Patients then recorded their pain and expectation scores at home for 10 days. This was the average of the pain that the patients experienced before, during and after defecation or the average of the pain during the course of the day. Two patients failed to return their 10 day pain scores [7%].
Pain scores were recorded on a ten-point Visual-analogue scale with scores from 1 to 10, with 1 being 'no pain' and 10 being 'as bad as it could be'. Ten-point patient expectation score was -5 to 5 with -5 being 'much better than expected' and 5 being 'much worse than expected'. Seven point satisfaction score was -3 to 3 with -3 being 'extremely dissatisfied' and 3 being 'extremely satisfied'.
Clinical follow-up by the surgeon (NGR) at 10 days, 6 weeks and 6 months evaluated the surgical outcome and recorded all surgical complications. Patients sent their satisfaction scores directly to the research nurse at these time-points and were un-influenced by the surgical out-patient visit.
All haemorrhoidectomies [Park's modified Milligan-Morgan technique13] were performed by a single surgeon [NGR]. Prone-Jacknife position (with buttocks strapped apart) was used for those randomised to local anaesthesia while Lithotomy-Trendelenburg position was used for those undergoing the procedure under general anaesthesia. Those with Type B and C buttocks10 needed more Trendelenburg position.
Perianal block was used for all patients irrespective of their randomisation. GH were given the block prior to commencement of surgery. This was performed with 20 ml of 1% Lignocaine (with 1 in 10000 Adrenaline) injected at four sites [midline anterior and posterior; left and right lateral], fanning the needle in three directions at each of the four sites; care being taken to inject outside the external sphincter, to avoid pain. Once the sphincter muscle relaxed with the perianal block, a further 10 ml of the same anaesthetic was injected submucosally raising a bleb in each of sites corresponding to the sites of perianal block. This bleb was massaged inferiorly. No sedation was used with local anaesthetic haemorrhoidectomy.
Following diathermy excision of haemorrhoids, a tube of lignocaine gel (Instillagel) was instilled into the anal canal followed by insertion of a gram of metronidazole and 50 mg of voltarol unless a history of asthma contraindicated the use of Voltarol in which case that was omitted. A soft sponge 'pack' [curisponge] was subsequently inserted. Patients were warned pre-operatively to expect the passage of the gelatinous curisponge in the post-operative period with their first defaecation.
A package of medications was given to take home (TTA). TTA contained Co-codamol, Ibuprofen, Metronidazole, Lactulose, Dulcolax, 5% lignocaine ointment and 2% Diltiazem cream, with detailed instructions on its usage. Message in the post-operative instruction leaflet was reiterated prior to discharge.
Journey time was calculated as the time elapsed between the start of anaesthesia and patient going home.
Infection was defined as presence of purulent discharge with heightened pain, a visit to their general practitioner and use of antibiotics over and above the Metronidazole prescribed on discharge.
Sum of the individual costs of the suture material, anaesthesia, cost of day surgery staff, recovery room costs and post operative medications were the basis of cost analysis.
Statistical analysis:
Data collected on Microsoft Excel was analysed on 'Analyse-it for Microsoft Excel' [Analyse-it Software Ltd, Leeds, UK]. Chi-square test and Mann-Whitney U test were used. Where the data was normally distributed as in the comparison of age, student's t-test was used. Serial measurements on linear analogue pain score were summarised by calculating the average pain over the 10-day time period for each patient as a summary measure14.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| 1 | Active comparator | Procedure: Hemorrhoidectomy30 ml of 1% Lignocaine with 1:10,000 Adrenaline |
| 2 | Active comparator | Procedure: HemorrhoidectomyStandard General anaesthesia with Enflurane and Propofol. |
Who may qualify
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Key inclusion criteria (1 listed)
- Third degree haemorrhoids
Key exclusion criteria (1 listed)
- Unfit for day-surgery or general anaesthesia.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| HemorrhoidectomyHemorrhoidectomy under local anaesthesia | Procedure or surgery | 1 |
| HemorrhoidectomyGeneral anaesthetic haemorrhoidectomy | Procedure or surgery | 2 |
Primary outcome
Average pain and expectation score.
Time frame: 6 months
1 secondary outcome
Journey time and cost analysis
Time frame: 6 months.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Sep 2023.
- Derived from this study: PubMed 18389499Kushwaha R, Hutchings W, Davies C, Rao NG. Randomized clinical trial comparing day-care open haemorrhoidectomy under local versus general anaesthesia. Br J Surg. 2008 May;95(5):555-63. doi: 10.1002/bjs.6113.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nagesh G Rao, FRCS, MD principal investigator
East Kent NHS Trust
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Hemorrhoidectomy in people with Hemorrhoids, run by East Kent Hospitals University NHS Foundation Trust at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 14 Sep 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Average pain and expectation score. (time frame: 6 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00503269, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Sep 2023.