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Postoperative Depression clinical trials

View clinical trials related to Postoperative Depression.

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NCT ID: NCT05625360 Recruiting - Anxiety Clinical Trials

REmotely-delivered Supportive Programs for Improving Surgical Pain and disTrEss

Start date: June 13, 2023
Phase: Phase 3
Study type: Interventional

The purpose of this research study is to learn how two different supportive programs may help women feel better after surgery. This study will measure if one type of supportive program is more useful than the other for improving wellbeing after surgery.

NCT ID: NCT05233566 Completed - Clinical trials for Postoperative Depression

Ketamine for Postoperative Avoidance of Depressive Symptoms: The K-PASS Feasibility Trial

K-PASS
Start date: April 25, 2022
Phase: Phase 3
Study type: Interventional

This protocol describes a feasibility trial that will evaluate the feasibility of conducting a full-scale phase 3 trial testing the hypothesis that a postoperative sustained, low-dose ketamine infusion can prevent postoperative depressive symptoms when administered to a targeted population of neurosurgical patients with a history of depression.

NCT ID: NCT05155969 Recruiting - Clinical trials for Postoperative Depression

Intravenous Esketamine on Prevention of Postoperative Depression in Patients Undergoing Cardiac Surgery

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

Esketamine is a general anesthetic with anti-depressant effects at subanaesthetic doses. This study hypothesized that intraoperative administration of ketamine would prevent or mitigate postoperative depressive symptoms in surgical patients.

NCT ID: NCT02452060 Completed - Pain Clinical Trials

Study on the Use of Low Dose Ketamine After Gastric Bypass and Gastrectomy

Start date: October 2014
Phase: Phase 2/Phase 3
Study type: Interventional

This is a randomized, double-blind, placebo-controlled, two-arm parallel, single-center study. One hundred subjects (50 in each arm) will be enrolled. Subjects, between the ages 18 and 65, undergoing laparoscopic gastric bypass or sleeve gastrectomy will be recruited and consented during the preadmission visit prior to surgery.