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Hemorrhoids clinical trials

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NCT ID: NCT00890721 Completed - Hemorrhoid Clinical Trials

Study of Pain Control in Hemorrhoidectomy

Start date: May 2009
Phase: Phase 3
Study type: Interventional

Patients will get an injection of either SKY0402 or placebo during hemorrhoid surgery, and their pain and pain medicine use will be monitored.

NCT ID: NCT00841620 Completed - Hemorrhoids Clinical Trials

Symptom Control 1-year After Circular Stapler Anopexy or Diathermy Excision for Prolapsed Haemorhoids

Start date: September 1999
Phase: Phase 4
Study type: Interventional

Background: In an international randomised controlled trial we studied how patient self-reported symptoms improved after either a stapled anopexy operation or a diathermy excision of the haemorrhoids. Methods: The study involved 18 hospitals in Sweden, Denmark and the UK. Two hundred and seven patients were randomised. After exclusion of 27 patients, 90 in both groups were operated and followed one year. Patients provided self-reported symptoms before surgery and after 1 year. A patient diary obtained daily self-reported postoperative pain scores (VAS). Surgeons evaluated the anal anatomy before surgery and after 1 year.

NCT ID: NCT00744848 Completed - Hemorrhoids Clinical Trials

Study to Evaluate Postoperative Analgesia in Subjects Undergoing Hemorrhoidectomy

Start date: August 2008
Phase: Phase 3
Study type: Interventional

Effective postoperative pain control to promote improved healing, faster patient mobilization, shortened hospital stays, and reduced healthcare costs.

NCT ID: NCT00717782 Completed - Clinical trials for Thrombosed External Hemorrhoid

Pain Relief for Thrombosed External Haemorrhoids

Start date: January 2003
Phase: Phase 4
Study type: Interventional

Thrombosed external haemorrhoids are one of the most frequent anorectal emergencies. They are associated with swelling and intense pain. This study evaluated the efficacy and safety of an intersphincteric injection of botulinum toxin for pain relief in patients with thrombosed external haemorrhoids

NCT ID: NCT00693459 Completed - Hemorrhoids Clinical Trials

Study of a New Circular Anal Dilator

Start date: May 2008
Phase: N/A
Study type: Interventional

The purpose of this research study is to test the effectiveness of a new anoscope used while performing a traditional hemorrhoidectomy.

NCT ID: NCT00630669 Completed - Hemorrhoids Clinical Trials

Comparison Between Two Endoscopic Treatments of Bleeding Internal Hemorrhoids:Band Ligation and Electrocoagulation Probe

Start date: December 1997
Phase: N/A
Study type: Interventional

The purpose of this study is to determine which treatment, band ligation (placing rubber bands around the hemorrhoids) or BICAP electrocoagulation (using electricity to cauterize) is safer and more effective endoscopic treatment for bleeding internal hemorrhoids.

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: 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.