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Hemorrhoids clinical trials

View clinical trials related to Hemorrhoids.

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NCT ID: NCT00617448 Completed - Hemorrhoids Clinical Trials

Ligasure Versus Diathermy Haemorrhoidectomy Under Local Anesthesia

LDHLA
Start date: May 2005
Phase: N/A
Study type: Interventional

The objective of this prospective randomised trial was to compare the short- and long-term efficacy of conventional diathermy haemorrhoidectomy versus Ligasureā„¢ diathermy, and to assess the short-term outcome of each procedure performed either under spinal anaesthesia or local anaesthesia with pudendal block with ropivacaine combined with intravenous sedation. We think, Ligasure haemorrhoidectomy under local anesthesia can be performed as day-case procedure and with equal results at long-term than conventional diathermy (considered goal standar of haemorrhoidectomy).

NCT ID: NCT00512044 Withdrawn - Hemorrhoids Clinical Trials

Local Versus General Anaesthesia in Stapled Hemorrhoidectomy

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether local or general anaesthesia in stapled hemorrhoidectomy leads to a shorter operation time with a better patient comfort.

NCT ID: NCT00503269 Completed - Hemorrhoids Clinical Trials

Local Anaesthetic Day-care Haemorrhoidectomy Challenges Traditional Concepts - a Randomised Controlled Trial

Start date: July 2005
Phase: N/A
Study type: Interventional

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.

NCT ID: NCT00487045 Completed - Hemorrhoids Clinical Trials

Prevention and/or Reduction of Hemorrhoids and/or Thrombosed External Hemorrhoids Using the HEM-AVERT Perianal Stabilizer Instrument

HEM-AVERT
Start date: December 2007
Phase: Phase 1
Study type: Interventional

This study is being conducted to evaluate an investigational instrument called the HEM-AVERT Perianal Stabilizer and its efficacy in reducing the occurrence or severity of hemorrhoids and thrombosed external hemorrhoids (TEH) which commonly occur during vaginal delivery.

NCT ID: NCT00405288 Completed - Pregnancy Clinical Trials

The Safety of Proctofoam-HC in the Third Trimester of Pregnancy

Start date: November 2006
Phase: Phase 4
Study type: Observational

The purpose of this study is to evaluate the fetal safety of topical application of Proctofoam-HC®, an antihemorrhoidal, in the third trimester of pregnancy.

NCT ID: NCT00397137 Completed - Hemorrhoids Clinical Trials

Stapled Anopexy Versus Closed Haemorrhoidectomy for Haemorrhoids

Start date: September 2000
Phase: N/A
Study type: Interventional

The aim of this study is to determine the role of stapled anopexy in the treatment of haemorrhoids by comparing it to the current gold standard treatment, which is excisional haemorrhoidectomy.

NCT ID: NCT00354029 Completed - Pain Clinical Trials

Effect of Perioperative i.v. Low-dose S(+) Ketamine

Start date: August 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether the use of perioperative intravenous S (+) ketamine reduces the amount and degree of postoperative pain. Furthermore the purpose of this study is to determine whether the use of perioperative intravenous S (+) ketamine effects cognitive function in the early postoperative period.

NCT ID: NCT00328900 Unknown status - Hemorrhoids Clinical Trials

Measurement of Stress During Anesthesia With "Pain Detector" on Patients Receiving Atropine

Start date: January 2006
Phase: N/A
Study type: Interventional

24 patients randomly divided into two groups, one of the groups receiving atropine in addition to the planned anaesthesia. Skin conductance parameters to be compared between the two groups.

NCT ID: NCT00160290 Terminated - Hemorrhoids Clinical Trials

Trial to Evaluate Effect of Lactulose on Hard Stools in Patients With Hemorrhoids or Anal Fissures

Start date: March 2002
Phase: Phase 4
Study type: Interventional

To demonstrate that lactulose acts as a stool softener, relieving the pain at defecation, improving the number of defecations and regulating the colonic transit time in patients suffering of hemorrhoids or anal fissure. To compare efficacy and quality of life in patients treated either with lactulose or plantago ovate.