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Postoperative Complications clinical trials

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NCT ID: NCT02548715 Withdrawn - Neoplasms Clinical Trials

Levothyroxine Treatment for Subclinical Hypothyroidism After Head and Neck Surgery

LSHT
Start date: July 2015
Phase: Phase 2/Phase 3
Study type: Interventional

Patients that require treatment for cancers of the head and neck often require a combination of surgery and/or radiation and chemotherapy. Hypothyroidism is one of the most common complications, and has been associated with post-operative complications such as wound healing problems, fistula formation, and decreased quality of life and survival. Several studies have examined hypothyroidism after radiation to the head and neck, but few have examined this after non-thyroid head and neck surgery. Head and neck resection is theorized to devascularize the thyroid, thus resulting in post-operative hypothyroidism. Synthroid is a synthetic thyroid hormone often used in cases of patients with proven hypothyroidism and after surgical thyroid removal. It's use has been in effect and studied for over fifty years. Treatment algorithms for hypothyroidism are well published. However, treatment of subclinical hypothyroidism (elevated TSH with normal or near-normal T3/T4) is controversial. The rate of subclinical hypothyroidism after non-thyroid head and neck surgery is high (up to 20%), and is associated with post-operative complications as noted above. Therefore the investigators propose a double blinded randomized controlled trial comparing outcomes of patients that develop subclinical hypothyroidism after head and neck surgery, who are given a standardized dose of synthroid treatment versus those treated with placebo. The main outcomes to be examined are post-operative complications (wound healing issues, fistula formation), survival, and quality of life measures.

NCT ID: NCT02019342 Withdrawn - Stroke Clinical Trials

Study to Determine the Impact of Intraoperative Blood Pressure Management on Postoperative Outcomes (MAP-ALIVE)

MAP-ALIVE
Start date: June 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine 1. whether intraoperative hypotension or hypertension is independently associated with postoperative mortality and morbidity 2. whether quality improvement interventions implemented at the University of Michigan and at Washington University: 1. decrease the extent and duration of intraoperative hypotension and hypertension. 2. are associated with decreased postoperative mortality and morbidity.

NCT ID: NCT01340742 Withdrawn - Clinical trials for Perioperative/Postoperative Complications

Remote Ischemic Preconditioning Before Abdominal Surgery

Start date: June 2010
Phase: N/A
Study type: Interventional

Major abdominal surgeries are associated with perioperative cardiac morbidity of up to 10%. Ischemic preconditioning may have a protective effect. The purpose of this study is to find out remote ischemic conditioning by inflating a blood pressure cuff on the arm will have a protective effect.

NCT ID: NCT00789659 Withdrawn - Wound Infection Clinical Trials

Incisional Wound Vac in Obese Patients

Start date: December 2010
Phase: N/A
Study type: Interventional

It is the belief of the investigators that the current trends in complication rates associated with fixation of pelvic ring injuries and acetabular fractures in the obese are unacceptable. The overwhelming majority of these complications can be attributed to problems with surgical wound healing. The investigators feel that if a cost effective and easily performed intervention can be prospectively utilized in a specific at-risk orthopaedic trauma population in order to control a potentially devastating complication, then efforts in discovering such an intervention may prove valuable. It is our hypothesis that obese patients treated with V.A.C. therapy after standard closure of trauma-related, operative orthopaedic incisions will have fewer postoperative wound complications.

NCT ID: NCT00511212 Withdrawn - Clinical trials for Postoperative Complications

Intravenous Immunoglobulin in Combination Therapy With Antibacterial Agents for SSI of the Lower Digestive Tract

Start date: August 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the clinical usefulness of IVIG in combination therapy with antibacterial agents for severe peritonitis after lower digestive tract surgery.

NCT ID: NCT00455182 Withdrawn - Pain Clinical Trials

Acupuncture for Pain Management After Hip or Knee Arthroplasty

Start date: March 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether patients treated with acupuncture post-operatively following knee or hip arthroplasty achieve better pain control as measured by the Visual Analog Scale and pain medication use.