Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01902966 · ClinicalTrials.gov registry record · NA

Feasibility - Beta Adrenergic Blockade (BB) in Cervical Cancer (CX)

A NA study, sponsored by M.D. Anderson Cancer Center.

Terminated
Registry status
NA
Development phase
6
Enrollment target

NCT01902966: Clinical Trial NA study, sponsored by M.D. Anderson Cancer Center.

NCT01902966 is a NA study that was terminated before completion, run by M.D. Anderson Cancer Center. The registered enrollment target is 6 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist → Add completion date to calendar (.ics) →

The verdict

NCT01902966, a NA study, was terminated before completion, sponsored by M.D. Anderson Cancer Center.

TERMINATED
Registry status
NA
Development phase
6 participants
Enrollment target

Study Summary

The goal of this clinical research study is to learn how many patients with advanced, recurrent, incurable cervical cancer will complete questionnaires about symptoms, any anxiety, depression, and/or pain, and the quality of their lives. Researchers also want to learn how many of these patients will complete a study treatment of propranolol hydrochloride and relaxation and guided imagery sessions. Researchers also want to learn if and how propranolol hydrochloride and relaxation and guided imagery may affect cancer symptoms and any anxiety, depression, and/or pain, and quality of life. Propranolol hydrochloride is designed to block certain chemicals that affect the heart. Relaxation and guided imagery sessions are a form of relaxing meditation that involves tensing and relaxing various parts of your body from your feet to your head. In the guided imagery portion, you listen to recordings that are designed to help with calmness, control, and decreasing stress.

Primary Outcome

To determine the proportion of patients completing symptom inventory, anxiety and depression survey, pain inventory, and quality of life surveys (MDASI, HADS\< BPI, FACT-Cx).

Interventions

  • BEHAVIORAL Questionnaires
  • DRUG Propranolol
  • BEHAVIORAL Diary
  • BEHAVIORAL Relaxation Audio Recording

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2013-09-11
Est. Completion 2020-08-14
Phase NA
M.D. Anderson Cancer Center

2,692 total trials

Why NCT01902966 stopped before completion

NCT01902966 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 4 interventions - of which Questionnaires is the first listed.

NCT01902966 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01902966 about?

NCT01902966 is a clinical study titled "Feasibility - Beta Adrenergic Blockade (BB) in Cervical Cancer (CX)". The goal of this clinical research study is to learn how many patients with advanced, recurrent, incurable cervical cancer will complete questionnaires about symptoms, any anxiety, depression, and/or pain, and the quality of their lives. Researchers also want to learn how many of these patients will...

What is the current status of trial NCT01902966?

This trial is currently terminated. It is a NA study. The enrollment target is 6 participants. The study started on 2013-09-11. Estimated completion is 2020-08-14.

What interventions are being tested in trial NCT01902966?

The interventions under investigation include: Questionnaires (BEHAVIORAL), Propranolol (DRUG), Diary (BEHAVIORAL), Relaxation Audio Recording (BEHAVIORAL).

Who is sponsoring clinical trial NCT01902966?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01902966's enrollment target sits among peer trials

6 1983rd of 2000 higher than 13 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01902966, the US trial registry maintained by the National Library of Medicine. NCT01902966 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.